Male Infertility Treatment Delhi India Doctor Specialist Hospital Centre Clinic Best Most Famous Experienced Senior Expert Guaranteed Cause Diagnosis Investigations East West North South Central Noida Ghaziabad Faridabad Gurgaon

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Male Infertility
Female Infertility
Pituitary Disorder 
Low Blood Sugar 
Cushing's disease
Calcium disorder/ Parathyroid Level
Rickets & Osteomalacia
Osteoporosis 

 

 

Pituitary  Disorder

 

  Growth Hormone Disorders
Hyper Prolactinemia
Hypopituitarism
Diabetes Insipidus
 

Pituitary is a hormone producing gland situated in brain. It makes hormones as L.H., F.S.H., Prolactin, T.S.H., A.D.H. etc. Various disorder of Pituitary are pituitary Tumours & pituitary failure. Pituitary Tumours: It can be microdenoma i.e. small Tumour or macro adenoma i.e. large Tumour. It can be hormone secreting as GH Secreting (Acromegaly), Prolactin Secreting (microprolactinoma, marcoprolaetinoma) very rarely it can be cancerous. There is a Tumour called craniopharyngioma it is non pituitary Tumour which behaves just like non-functional pituitary adenoma. Symptoms of pituitary Tumours are headache, decreased vision, sumptoms due to high GH as tall height & pituitary deficiency etc.   

Growth Hormone disorders :
Acromegaly :
Excess of growth hormone leads to disease called acromegaly. In this disease excess growth hormone production from pituitary Tumour (adenoma) or due to hyperplasia causes following symptoms : excess sweating, excess height gain in child, weight gain, heavy voice, tingling & numbness in hand or feet, prominence of facial bony prominences, cardiac enlargement & even heart failure, day time sleepiness snoring.  Diagnosis : Growth hormone testing before & after giving 100 gm. glucose.   
Treatment :
Growth hormone level needs to be normalized by surgery, various drugs or injection.   

Hyper prolactinemia (High prolactin hormone due to prolactinoma micro or macro). Causes of high prolactin are : Stress, milk feeding by mother (Lactation). 

Other cause :

Prolactinom
Acromegaly  
Cushing's disease
Hypothyroidism  
Pituitary tumour  
Hypothalmic disease
Empty Sella Syndrome  
Chest wall irritant lesions  
Drugs as antipychiatric drugs, TCA, Metoclopramide  
Renal, Liver disease
Idiopathic   

Symptoms : In women it causes menstrual irregularity as delayed & less period even absent periods, milk secretion from breast (Galactorrhoea), decreased desire for genital, infertility & recurrent abortions. In girls it may cause small breast. 

In males it leads to decreased desire, breast enlargement, decreased sperm count, Infertility. In young boys it may leads to absence of beard & moustache & small pennis. 

Treatment : There are many drugs which can cure, it in two month to six months time. Sometimes surgery is required or radiosurgery by Gamma knife i.e. surgery by rays without cutting the body or using the blade. 

Pregnancy & high prolactin (Prolactinoma micro & macro) In hyperprolactinema women becomes pregnant only when serum prolactin is normalized. Once pregnancy is confirmed then  Bromocriptine (proctinal/sicryptin) or cabergoline (Caberlin) should be stopped, if there is no evidence of local Tumour compression. If tumour enlarges & produces compressive signs then antiprolactinemic therapy should be restarted. 

Stopping of Lactation : After delivery of body due to some reasons as mother living away from baby or death of baby there are certain drugs which stop milk secretion. 

Medicines to start lactation i.e. milk secretion are available.

Hypopituitarism

Hypopituitarism : i.e. deficiency of   pituitary hormones. Symptoms of pituitary deficiency are short height in child, signs of hypothyroidism, Addison disease, weight gain or loss, psychiatric disorders, darkening of  skiin, weakness, dry skiin & hair loss. Giddiness on standing, fall of auxiliary  & pubic hair, genital failures & Infertility : Causes of hypopituitarism are 

Causes of hypopituitarism

Infarction : Postpartum necrosis (Sheehan syndrome), Vascular disease (in diabetes mellitus), Head trauma
Infections : Tuberculosis, Fungi, Pyogenic, Syphilis, Toxoplasmosis
Granulomas, Saroidosis, Langhans cell histiocytosis
Autoimmune lymphocytic hypophyysitis
Neoplasms involving pituitary : Pitutitary adenoma, Vraniopharyngioma, Metastatic or primary carcinoma (rare)
Aneurysm of internal carotid artery, Hemochromtosis
Idiopathic or genetic disorders : Deficient production of pituitary hormone, Synthesis of abnormal hormone,

Primary hypothalamic disorders : Tumours (e.g. cranipharyngiome, glioma), Granulomas (sarcoidosis, langhans cell histiocytosis), Midline central nervous system structural anormalies of hypothalamus, Genetic or idiopathic releasing hormone deficiency, Head trauma

Latrogenic factors : Stalk section, Radiation, Hypophysectomy 
Treatment is replacement of deficient hormones & treatment of cause.   

Diabetes Insipidus

Diabetes Insipidus is called when patient passes too much urine i.e. he has to go for urination frequently, causes for it are vasopressin deficiency due to hypothalamic, pituitary disease as Idiopathic, Tumours, croniopharyngioma, histiocytosis X, inflammatory disease. It can also be due to renal diabetes (Nephrogenic diabetes insipidus, hypercalcemia,  hypokalemia). Sometime it can be due to primary polydypsia or due to certain drugs. Sometime diabetes insipidus can occur during pregnancy due to certain cause. 

Causes of central diabetes indipdus

Primary causes (not acquired) : Familial (autosomal dominant), Idiopathic
Secondary Causes (acquired) :
Traumatics :
Accidental (i.e. head trauma), Latrogenic (i.e. surgery)
Tumours :
Craniopharyngioma, Primary pituitary tumors, Metastatic disease (breast cancer, lung cancer), Acute leukemia, Lymphomatoid granulomatosis, Ratyhke cleft cyst
Mixed germ cell tumor (rare), Granulomatous disease, Sacroidosis, Hystiocutosis
Tuberculosis,
Infection diseases :
Meningtis, Encephalitis,
Vascular :
Aneurysms, Sheehan syndrome, Hypoxic encephalopathy
Drugs :
Alcohol, Diphenylhydantoin
Autoimmune :
Lymphotic hypophysitis (rare; usually affects anterior adenohypophysis) 
Hereditary :
Familal X-linked recessive (mutation in V2 receptor), Autosomal recessive (mutation in aquaporin gene), Autosomal dominant (mutation in aquaporin gene)
Acquired : Drugs : Lithium therapy (inhibit production cAMP? Disruption in short and long-term, Regulation of AP), demeclocycline, methoxyflurane, Metabolic : Hypokalemia (decrease sensitivity of adenylycyckase to ADH, affects, only long-term regulation of AP-2), ADH-induced AP-2 regulation via apical calcium sensor receptor), Postbilateral ureteral obstruction BPH and neurogenic bladder (impaired long-term AP-2, regulation only), Vascular: sickle cell disease or trait, Infiltrative : amyloidosis, Low-protein : diet
These are easily treatable.

Low blood sugar (Hypoglycemia)

What is Hypoglycemia?
Causes 
Investigations & Diagnosis
Treatment
Why Doctors miss it
Response of treatment
Side effects of treatment
Other important informations

Hypoglycemia is called when blood sugar becomes below normal. In hypoglycemia patient has recurrent symptom of weakness, anxiety, confusion, cold feeling, headache, vomiting. Causes of low blood sugar (glucose) are : 
(1) High insulin level in blood due to pancreatic tumor as insulinomas or other cause.
(2) Due to various drugs
(3) Deficiency of various hormones as cortisol, growth hormone.
(4) Other congenital defect as galactosemia.
(5) Other causes as alimentary hypoglycemia & Idiopathic postprandial hypoglycemia.
(6) Autoimmune cause. 

Postprandial: Alimentary, Impaired glucose tolerance, Diet induced, Idiopathic, Postabsorptive hypoglycemia, Endocrine deficiencies, Alcohol, Insulin antibodies
Post absorptive, Insulinomas, Factitious, Insulin, Sulfonylureas

Autoimmune : Insulin antibody, Insulin receptor antibody, Nonislet cell neoplasms
Hormonal deficiencies, Adrenal, pituitary, thyroid, Glucagon
Liver disease-severe: Cirrhosis with speticemia
Inadequate substrate for gluconeogenesis : Uremia, , Alcohol, Drugs 

Diagnosis : We do blood sugar, plasma insulin level which may be high or low, other hormone, GTT, Abdomen ultrasound to reach proper diagnosis then treatment of the cause is done. 
Low blood sugar/glucose in child can be due to neonatal hypoglycemia, hyper insulinemia & other causes. So permanent Treatment :cure of low blood sugar needs accurate diagnosis & then appropriate treatment .
Causes of high insulin are
Pancreatic beta cell tumour called insulinoma.
Insulin resistance, PCOD, Hairan Syndrome Syndrome X
Excess of cortisol & growth hormones.
Anti insulin Antibody. Anti insulin receptor antibody.
& Many more other causes. 
How to avoid Severe Hypoglycemia In Diabetes 

• Don’t make changes in Diet, insulin dose, exercise yourself. 
• Don’t forget to take meal & snacks at proper time
• Take extra snacks before doing unusual exercise.
• Take glucose on slightest symptom.
• If on insulin keep inj. Glucagon (s.c./IV) to treat hypoglycemia.
• Avoid Night-time Hypoglycemia : Nightmares, excess sweating at night, early morning 
headache, for confirmation 3 AM Blood sugar below 60.
• Treatment of severe hypoglycemia : Inj. Glucagon s.c. or shift to hospital for intra venous 
Glucose. 

Adrenal Steroid Hormones (Cushing’s Disease)


In some diseases Adrenal hormone cortisol increases (called Cushing’s disease or syndrome) it leads to weight gain, high blood pressure, stretch marks over body, unwanted hair in female, osteoporosis, weakness, fatigue, roundening of face, thin ness of hand & feet, reddening of cheek, development of high blood pressure & diabetes, darkening of skiin & abdominal protuberance.. Some similar conditions are called pseudo Cushing’s syndrome. There are certain steroid hormone tablets when they are taken orally it leads to weight gain & has lot many more side effects & produce features like Cushing’s syndrome.. When cortisol decreases due to adrenal failure called Addison’s disease the symptoms are darkening of skiin, weight loss, weakness, Giddiness, loss of appetite, vomiting, muscle or joint pains, low blood pressure (hypotension), high sodium, low potassium, high urea, & high calcium for treatment adequate dose of predinisolone & dexamethesone, sometime fludrocortisione is also needed one must know in detail steroid replacement therapy. 

Similarly aldosterone can increase or decrease. 

Congenital adrenal hyperplasia leads to enlarged clitoris in female & development of early pubic hair in male & female, also leads to unwanted hair in female. For diagnosis & monitoring 17 hydroxyprogesterone & other hormones are tested which can be elevated or subnormal. 
Adrenal gland enlargement, (tumors), can also be noted. 
High Blood pressure due to hormone disorder like pheochromocytoma & other hormone disorder is well known. Pheachromocytoma presents with uncontrolled blood presure, headache, palpitation, anxiety. 
Investigation : Urinary Catecholamines, metanephrines & vanilmandellic acid (VMA) are increased then C.T. Scan abdomen & MIBG scan are required. 
Treatment : Certain drugs are effective otherwise surgery is needed. 
Diagnosis : For diagnosis we need hormone test as LH, FSH, Testostrone, Prolactin, Thyroid tests, Antisperm antibody, X-ray skull, USG of Scrotum & Semen C/S to reach correct diagnosis of low sperm count. 
Treatment : Once the cause of low sperm count & motility found then with three months of treatment sperm count becomes normal 

Increased Calcium Level/Parathyroid Level 

What is High calcium / high PTH
Causes 
Investigations & Diagnosis
Treatment
Why Doctors miss it
Response of treatment


Hypercalcemia i.e. increased Calcium Level is called when serum calcium is above normal. Symptoms of elevated calcium due to high PTH level i.e. hyperparathyroidism is excess urination, kidney stone, bone weakness, osteoporosis, bone pains & muscle weakness This is caused by following causes hyperparathyroidism (i.e. high Parathyroid (PTH) hormone), high level of Vitamin D, familial hypercalcemia, multiple endocrine neoplasia Type-I, various malignancies as breast cancer, multiple myeloma & other malignancies without bone metasis, Ectopic high P.T.H. production, thyrotoxicosis, Hyper Vitaminosis A, Sarcoidosis, milk alkali syndrome, Thiazide diuretics, acute renal failure etc. 

Diagnosis of cause of high/elevated calcium, one need to calculate corrected calcium levels, test PTH hormone, parathyroid scanning & urinary calcium testing. 

Treatment :
Find out any one of the above cause & treat. Regarding treatment of
hyperparathyroidism there are various drugs which lower calcium value & even PTH value or surgery can be done. 

Low i.e. Decreased calcium (hypocalcemia)

What is Hypocalcemia
Causes 
Investigations & Diagnosis
Treatment
Why Doctors miss it
Response of treatment

is called when serum calcium is below normal. Symptoms of low calcium are spasm of hand & face muscles ie. tetany, early cataract, abnormal body movements, dry skiin, constipation, anxiety & depression. Subnormal calcium is caused by hypoparathyroidism, pseudohypoparathyroidism, Vitamin-D deficiency, & vitamin D. Resistance, postsurgical, idiopathic, hypomanesemia wilson disease, pancreatitis, acute hyperphosphatemio, any serious critical illness, toxic shock syndrome, malabsorption, calcium chelators. 
Neonatal hypocalcemia can occur in newborn.
 
Diagnosis all above causes diagnosed by investigation of calcium, protein, albumin, parathyroid hormone level & urinary calcium excretion. 

Treatment is possible by treating the cause & supplementing calcium, Vitamin D & others. 
Phosphorus can be high or low due to various metabolic causes.

Rickets & Osteomalacia :


means bone weakness due to less bone formation. Rickets occurs in children & ostcomalacia in adult. The symptoms in child are bone pain, short height, difficulty in walking. In adults osteomolacia presents as bone pain, difficulty in standing from sitting posture. 
Causes of osteomalacia, rickets & elevated alkaline phosphatose are Vitamin D deficiency & Resistance, hypophosphatemic rickets, chronic renal disease & failure, Renal tubular acidosis, fanconi syndrome, Tumoural osteomalacia etc. 

Diagnosis : On Laboratory testing calcium & phosphorus may be low, alkaline phosphatase high & bone is weak on X-ray, PTH level & other relevant test are done.

Treatment : Once the cause is found, treatment can be successfully done by treating the cause & supplementing calcium & Vitamin D 

Osteoporosis i.e. Bone Weakness 


Osteoporosis i.e. bone weakness occurs due to excess bone loss, is very common after 50 years of age. It leads to frequent fracture of spine bone & leg bone on minor trauma. 

Cause of osterporosis are estrogen deficiency, hyperparathyroidism, vitamin D deficiency, multiple myeloma, idiopathic, calcium deficiency, cortisol excess, steroid use, chronic inflammatory disease as rheumatoid arthritis, SLE, malabsorption syndrome, thyrotoxicosis, hypogonadism, hyperprolactinemia, cancers, Liver disease, alcohol use, juvenile osteoporosis. 
In male all above cause plus testtosterone deficiency due to hypogonadism is an additional cause for osteoporosis.
 
Dignosis : By various blood test & dexa bone denistometry scan then diagnosis is made. Dexabone scan shows osteopenia i.e. low T score & Z score. 
Treatment offered is treatment of cause, calcium, Vitamin D, female hormone, raloxifene, Tibolon & Biphosphonates & synthetic PTH given with good results. 

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We get patients from all major cities in India & Abroad . In the following cities all the facilities for investigation & treatments including medicines are available as Delhi (North, South, East, Central, West, New Delhi), Ghaziabad, Faridabad, Noida, Gurgaon, Meerut, Saharanpur, Dehradun, Ferozepur , Aurangabad, Manesar, Rewari, Pataudi, Rohtak, Bahadurgarh,Bombay,  Bhiwani, Karnal, Panipat , Ambala, Ludhiana, Amritsar, Batala, Gurdaspur, Jalandhar, Patiala, Chandigarh, Calcutta,  Ferozepur Simla, Manali, Jammu, Udhampur, Poonch, Rajouri, Srinagar, Kargil, Aligarh, Mathura, Etawah, Lucknow, Kanpur, Allahabad, Varanasi, Kashi, Faizabad, Bareilly, Moradabad, Rampur., Dehradun, Uttarkashi, Meerut, Sitapur, Mathura,  Madras, Pilibhit, Nainital, Almora, Agra, Ferozabad, Jhansi, Alwar, Jaipur, Dausa, Ajmer, Beawar, Pali, Bhilwara, Chittorgarh, Kota, Dholpur, Churu, Ratangarh, Sikar, Bikaner, Jodhpur, Jalore, Rajkot, Porbandar, Jamnagar, Dwarka, Junagadh, Surendranagar, Bhav Nagar, Ambala, Ahmedabad, Gandhi Nagar, Godhra, Vadodara, Surat, Bilmora, Navasari, Mumbai, Sonapur, Kalbadevi, Girgaon, Dadar, Mahim, Dharavi, Juhu, Andheri, Kurla, Sahar, Pune, Thane, Palghar, Panaji, Panvel, Solapur, Pandharpur, Ahmednagar, Satara, Kolhapur, Ichalkaranji, Kalyan, Nasik, Dhule, Bhir, Nagpur, Bhandara, Amraoti, Khandwa, Indore, Ujjain, Ratlam, Mandsaur, Bhopal, Vidisha, Sagar, Guna, Shivpuri, Gwalior, Jabalpur, Bhilai, Raipur, Hyderabad, Zahirabad, Suryapet, Guntakal, Chittoor, Tirupati, Tirumala, Nandyal Vijayawada, Guntur, Goa,  Tenali, Nellore, Visakhapatnam, Vellore, Bangalore, Banglore, Ulsoor, Mysore, Srirangapatna, Hassan, Mangalore, Udupi, Manipal, Davanagere, Shimoga, Dharwad, Hubli, Bellary, Hospet, Bijapur, Belgaum, Chennai, Chengalpattu, Pondicherry, Tiruvannamalai, Kumbakonam, Thanjavur, Tiruchirappalli, Palani, Madurai, Sivakasi, Tirunelveli, Ambasamudram, Tenkasi, Nagercoil, Kanchipuram, Salem, Erode, Tirupur, Coimbatore, Pollachi, Kanyakumari, Ernakulam, Trivandrum, Calicut, Kottayam, Calcutta, Howrah, Purulia, Darjeeling, Siliguri, Gangtok, Bhubaneswar, Puri, Rourkela, Guwahati, Shillong, Imphal, Kohima, Agartala, Patna, Gaya, Bokaro, Jamshedpur, Ranchi, Madhubani.

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 At these places all the facilities for investigation & treatments are available.

At our center / centre / clinic / clinics / hospital / hospitals doctors are dedicated for latest & scientific treatment of these diseases.

Electrolytes, Bicarbonate and lipid profile mini), IBD profile, serum (Inflammatory Bowel Disease) (MPO-ANCA, PR3 ANCA, ASCA-lqG and IqA), IgA, IgE, serum, IgG, IgM, IGF BP-3, serum, IGF-1 (Somatomedin C), serum, IHA for Amoebiasis, IL-1 alpha receptor, IL-1 beta receptor, IL-10, IL-2, IL-3, IL-4, IL-3, IL-4, IL-5, IL-6, IL-8, Immunofixation, Qualitative (Includes protein electrophoresis and Immunofixation), Immunofixation, Quantitative (Protein Electrophoresis, quantification of heavy & light chains & Immunofixation), Immunoglobulin profile, profile (FSH, LH, Prolactin, Testosterone, SHBG, Free Androgen Index), India Ink Preparation, CSF, Infectious Mononucleosis test, serum, Infertility profile (Male) (CBC, FBS, PPBS, BUN, Urine it, Semen rt, FSH, LH, Prolactin, Testosterone, ASAB, Chlamydia IgG/lgA), Infertility profile, Female (CBC, FBS, PPBS, BUN, Urine rt, Blood group, FSH, LH, Prolactin, TSH, ASAB, Chlamydia IgG/lgA), Influenza A & B, IgM Antibody, Insulin antibody, Insulin, serum, Insulin Suppression test for C-peptide test (FastingI & post insulin (0.1 U/Kg of body wt) samples at 10,20,30,40,50,60 Minutes), Interferon Gamma, Intrinsic factor antibody, serum, ionised calcium, serum, Iron, Iron studies, Serum, Islet cell antibody, serum, Isospcra, stool, Jo-1 antibody, serum, Karyotyping (Giemsa banding) (G banding) (For numerical and structural chromosomal abnormalities), Karyotyping-High resolution banding, Kappa light chain, serum, Kappa/Lambda light chains, KCT-Kaolin Clotting time, plasma, Ketone bodies, urine, Ki-67, KOH mount, La Antibody SSB (Soluble substance B), serum, LAC (Lupus Anticoagulants) (screen), plasma, Lactate, Lambda light chain, serum, Lamotrigine, serum, Lanoxin (Digoxin), serum by CLIA, LDH Isoenzymes, serum, LDH-Lactate Dehydroqenase, LDL Cholesterol (Bad Cholesterol) (Direct), LDL Subtractions, LE Cell Detection, blood   , Lead, Lead poisoning tests, urine (ALA & PBG), Legionelta pneumophila IgM antibody, Leishmania antibody-IgG (for Kala Azar), Leptin (Human Leptin), Leptospira - IgG antibody, serum, Leptospira - IgM Antibody, serum, Leptospira, urine, Leucocyte Common Antigen by Immunohistochemistry, LH-Leutinising Hormone (Specific), serum, Lipase level, serum, Lipid profle, Max! (Cholesterol-total, HDL, LDL, VLDL and triglycerides, Lp(a), Apolipoproteins A1/B), Lipid profle, Mini(Cholesterol-total, HDL, LDL, VLDL, triglycerides), Lipids, total, Lipoprotein Electrophoresis, serum, Lipoprotein(a) , serum, Lithium level, serum (Collect 12hrs post medication), Liver biopsy with Reticulin and Trichrome stain, Liver function test (Bilirubin-total, direct and indirect, SGOT, SGPT, GGTP, Proteins, Alkaline phosphatase), Liver and Germ Cell Markers (AFP, HCG Beta), Liver Marker profile (AFP, CEA), LKM1-Antibodies to Liver Kidney Microsomes, serum, Lung Marker profile (NSE, CEA), Lupus Anticoagulants (LAC) (screen), plasma, Lyme disease (Borrelia Burgdorferi) antibodies screen, Lysozyme (Muramidase) by Immunohistochemistry, Magnesium, serum, Malaria by Real time PCR, blood, Malarial Antibody, blood, Malarial Antigen (Vivax & Falciparum), blood, Malarial Parasite, blood, Mammography, Manganese, Mantoux lest (Tuberculin test) (For walkins), Marijuana (Cannabis) (THC), urine (Qualitative),, Marijuana (Cannabis) (THC), urine (Quantitative), Masson Trichrome stain for histopathology, MCP-1, Measles (Rubeola) -IgG antibodies, Measles (Rubeola)-IgM antibodies, Measles (Rubeola) -IgM antibodies, Meningitis Panel (IgG & IgM antibody to Coxsackie,

Different Hospitals in india are: Moolchand Health Care, St. Stephen’s Hospital, Dr. Ram Manohar Lohia Hospital, G.B Pant Hospital, Lok Nayak Hospital, RG Stone Urological Reasarch Institue, Sir Ganga Ram Hospital, Jeevan Hospital, Deen Dayal Upadhyaya Hospital, Orthonova Hospital, Batra Hospital, Sahi Hospital, Indraprastha Apollo Hospitals, Holy Faimly Hospital, Jeevan Mala Hospital, Jaipur Golden Hospital, Lady Harding Hospital, Smt. Sucheta Kriplani Hospital, Mata Chanan Devi Hospital, Safdarjung Hospital, Mohindra Hospital, M.P Heart centre Hospital, Bara Hospital, Hindu Rao Hospital, Holy Angels Hospital, Shankar Hospital, Holy Family Hospital, Chopra Hospital, Escorts Hospital St. Stephen's Hospital, Vardaan Hospital, Visitech Eye Hospital, Vardhman Mahavir Medical College, Safdarjung Hospital, Lok Nayak Jai Prakash (LNJP) Hospital, Private Hospital, Guru Teg Bahadur Hospital, Kalra Hospital,  Bangalore Baptist Hospital, Bowring Hospital, B W Lions Eye Hospital, Bangalore Hospital, Bangalore Children's Hospital, Genesis Hospital, Lakeside Hospital, M G A Hospital, Mallya Hospital, Manipal Hospital, Sindhi Charitable Hospital, Yellamma Dasappa Hospital,  Sir Harkisandas Narottamdas Hospital, Prince Alikhan Hospital, Saifee Hospital, Breach Candy Hospital, Jaslok Hospital, Habib Ismail Hosptal, Kalajyot Hospital, Motiben Dalvi Hospital, Bombay Hospital, Corwest Jain Clinic Group of Hospitals, D.S. Kothari Hospital, Lotus Hospital, Elizabeth Hospital, Bhatia Hospital, The Bomanji Dinshaw Petit Parsee Hospital, Cumbala Hill Hospital, Noor Hospital, K.B. Haji Bachoali Charitable Ophthalmic & ENT Hospital, Bai Jerbai Wadia Hspital, Nawroji Wadia Maternity Hospital, Wadia Hospital, Yerla Medical Trust Hospital, Tarachand Bappa Hospital, Dhanwantari Hospital, Shri Samasta Parajiya Suvarna Hospital, Smt.B.C.J. General Hospital, Smt.B.C.J. General Hospital, Holi Spirit Hospital, Lilavati Hospital, The Bandra Holy Family Hospital, Raheja Hospital, Gurunanak Memorial Hospital, Ramakrishna Mission Hospital, Radhibai Watumull Global Hospital, BSES Hospital, Sushrut Hospital, LH Hiranandani Hospital, Maganlal Popatlal & Sarvoday Hospital, Rajawadi Municipal General Hospital, Shatabdi Hospital, KBB Hospital, V.N. Hospital, Dr.K.B. Babha Hospital, Cooper Hospital, Bhagwati Hospital, Sion Hospital, K.E.M. Hospital Nayar Hospital, Kama Hospital, G.T. Hospital, J.J. Hospital, Sr.George Hospital, Aliganj Hospital, Blue Cross Hospital, Getwell Hospital, Krishna Lok Hospital, Lucknow Hospital, Medwin Hospital and Health Centre, Vivekanand Hospital, G.M.Associate Hospital, Dufferin Hospital, Civil Hospital, Communicable/Infectious Diseases Hospital Lifeline Hospital and Heart Centre, Lucknow Hospital, Shalimar Hospital, Rajendranagar Hospital Tuberculosis Hospital, Lucknow Rajpoot Hospital, Nishat Hospital, Z A Chartable Hospital, Indira Gandhi Eye Hospital, Sitapur Eye Hospital, Awadh Hospital and Heart Centre, Balrampur Hospital, Cantonment General Hospital, Civil Hospital, Dr.Shyama Prasad Mukherjie Hospital, Fatima Hospital, G.M.Associate Hospital, K.K.Hospital, Veerangana Jhalkari Bai Female Hospital, Shekhar Hospital, Queen Mary Hospital, Osmania General Hospital, Gandhi Hospital, Government Maternity Hospital, Nilofar Hospital, Cancer Hospital, T.B. Hospital, Hospital for Mental Diseases, Sarojini Devi Hospital, Sundram Medical Foundation, Chennai. MIOT Hospital, Chennai. Apollo Hospital, Madras. Malar Hospital Limited, Gandhi Nagar Adyar, Chenni. Calcutta Medical College Hospital. N.R.S. Medical College & Hospital, Calcutta. R.G. Kar Medical College & Hospital, Calcutta. Calcutta National Medical College & Hospital, Instt. of Postgraduate Med. Education & Research, Calcutta Seth S.K.M. Hospital, Calcutta. Sambhu Nath Pandit Hospital, Calcutta. Lady Dufferinvictoria Hospital, Calcutta. Howrah General Hospital, Howrah, Hoogly Sadar Hospital, Hoogly, Chittaranjan Seva Sadan & Chittaranjan Cancer Hospital,  Ramakrishna Mission Seva Pratishthan General Hospital, Calcutta.

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psychogenic amenorrhea, periodic, hyposecretion , causes , immunoregulatory functions , lipoprotein metabolism, marijuana use , mean blood production rate , adrenal contribution , measurement , elderly, mechanism action , metabolic effects , metabolism, metabolism , 16alfa-hydroxylation , ta-hydroxylation , dialysis patients, excessive, liver disease , metabolites , urinary, measurement , mineralocorticoid activity , mineralocorticoid excess, negative feedback effects , HPA, obesity , parturition, plasma protein binding by, Cortisol (continued) plasma / serum level , Hypercortisolemia; Hypocortisolism adrenal insufficiency, adults, anorexia nervosa, asthmatic patient with hyperthyroidism, children, critical illness, acute versus chronic phase, Cushing disease, Cushing syndrome, depressed women, psychogenic amenorrhea, feasting, hypothalamic chronic anovulation, hypothyroidism, increased causes , depressed women, psychogenic amenorrhea,. exercise-associated amenorrhea, infancy childhood, measurement , with adrenal incidentaloma, interpretation , metyrapone , normal, normal values vs. women with PCOS or oophorectomy, pregnancy, regulation , renal failure, stress, postpartum period, protein binding by, PTH levels, reference values , resistance , , laboratory findings , primary, relative, secretion , age-related changes , autonomous, basal level , circadian rhythms , depressed women, psychogenic amenorrhea, critical illness, dopamine , , light-dark cycle , modulation by sleep circadian rhythmicity, periodic, pregnancy, regulation , rhythms , stress, substance P , thymus , starvation , structure , synthesis , inherited disorders . Congenital adrenal hyperplasia metyrapone , therapy with, adrenal insufficiency, stress , congenital adrenal hyperplasia, fertility, stress, tobacco use , urinary, elevated, exercise-associated amenorrhea, hypothalamic chronic anovulation, pregnancy, urinary free Cushing disease, Cushing syndrome, measurement , Cushing syndrome, interpretation , difficulties , normal values , test , Cortisol-binding globulin (CBG), plasma / serum level , pregnancy, Cortisol receptor(s) type 1, type 2, Cortisone. Glucocorticoid(s) absorption , equivalent glucocorticoid dose , glucocorticoid potency , half-life , metabolism , mineralocorticoid activity , replacement therapy with, structure , therapy with (Cortone acetate), actions , adverse effects side effects , dosage administration , indications , preparations , Cortisone acetate. Cortisone intramuscular absorption , bioavailability , Cortisone test expected response , method , special considerations / interpretation , substance measured , Cortistatin(s), biofunction(s) , amino acid sequence , rats, CST-29, rats, expression , somatostatin deficiency, Cortol, Cortolone, Cortone acetate. Cosyntropin orynebaacterium, acne , Corynebaacterium minutissimum, erythrasma caused by, diabetes, Cosentino, Francesco, osman, Felicia, Cosmid(s), contiguous DNA block (contig) map, Costimulation, definition , Costimulators, autoimmune disease, Cosynthesis, peptide, Cosyntropin (Cortrosyn), actions , adverse effects side effects , dosage administration , indications , preparations , Cosyntropin (Cortrosyn) stimulation test, with adrenal incidentaloma, adrenal insufficiency, assessment HPA function glucocorticoid-treated patients, Cosyntropin (Cortrosyn) test, critical illenss, low dose, pregnancy, Cotranslation, Cotton-wool spots, causes , diabeticretinopathy, Cough medication(s), iodine content , Counseling, with genetic diagnosis, Counterregulatory hormone(s). Cortisol; Epinephrine; Glucagon; Norepinephrine critical illness, IFN-yama , overproduction , diabetes secondary , plasma / serum level , fasting, Coupling hormone-receptor, receptor-effector, Coupling defect, Covalent modification, metabolic regulation , Cowden disease, thyroid cancer , Cow’s milk proteins, diabetes, Cox, Brain M., Coxsackie A9 virus, epididymoorchitis caused by, Coxsackie B virus epididymoorchitis caused by, hypothalamic-pituitary infection, pancreatitis, subacute thyroiditis, CPCT. Choline phosphate cytidyltransferase CPD syndrome, ocular involvement , C peptide (insulin), deficiency , degradation , climination half-life , hepatic extraction , immunoassay , plasma / serum level , diabetes, , fat redistribution syndrome, reference values , renal metabolism , C-19 progestins, endometriosis, C-21 progestins, endometriosis, CPT. Carnitine palmitoyltransferase Cranial irradiation, gonadotropin-dependent precocious puberty , Cranial nerve(s) computed tomographic anatomy , III (oculomotor), magnetic resonance imaging , palsy , causes , diabetes, IV (trochlear), pasly , causes , diabetes, palsy diabetes, with pituitary tumors, schwannoma , imaging , V (trigeminal) maxillary division , ophthalmic division , ophthalmic division , VI (abducens), palsy , causes , chiasmal syndromes, diabetes, VII, palsy , diabetes, Cranial neuropathy diabetes, radiosurgery meningioma , Craniocaudal axis, embryo, Craniocaudal groove, raniopharynegeal canal, Craniopharynegeal duct, Craniopharyngioma(s) adamantinomatous (adamantinous), histopathology , recurrence , adrenal insufficiency caused by, adults, surgery , age distribution , anatomic distribution , chiasmal syndrome caused by, children, clinical course , clinical features , cystic, imaging , intracavitary instillation radioisotopes , delayed puberty, diabetes insipidus caused by, differential diagnosis , epidemiology , estrogen receptors , hyperosmolar syndrome caused by, hypopituitarism with, imaging , incidence , local recurrence , mixed cystic solid, imaging , ocular manifestations , origin , papillary (squamous-papillary), epidemiology , pathology , pathogenesis , pediatric patients, surgery , pituitary abscess, pregnancy, prevalence , prognosis , radiation therapy , dosage administration , dose considerations , postoperative, radiosurgery , recurrence , radiation therapy , signs symptoms , solid, imaging , subtotal excision , surgery , morbidity mortality with, preoperative evaluation with,. radiation therapy, combined, results , transcranial approach , transsphenoidal approach , survival rate , total excision , morbidity mortality with, treatment , outcome , Craniotabes, Cravings, nutrient, endocrine brain , C-reactive protein critical illenss, hydrocortisone infusion , adrenal assessment, inflammatory response, Creatine, urinary, protein status , Creatine-height index, protein status ,. Creatine kinase BB, plasma / serum level acromegaly, hypophosphatemia, hypothyroidism, neuromuscular disorders, Creatine phosphokinase elevation , idism, plasma / serum level , hypothyroidism, serum level , thyroid function , Creatinine rement , plasma / serum level , measurement , patient with nephrolithiasis, reference values , nary measurement , patient with nephrolithiasis, neonates, CREB. cAMP response element-binding protein CREB-binding (CBP), Crede maneuver, Creeping thyroiditis, Cre-Lox technique, Creombinants, Crerecombinase-loxP system, conditional (developmental) interruption gene expression, Cretinism, cataract formation, cerebral effects , characteristic facies , cutaneous manifestations , definition , dental / orofacial abnormalities , endemic, historical perspective , myxedematous, ocular manifestations , radic, Creutzfeldt-Jakob disease genotype , growth hormone therapy , human growth hormone therapy , human pituitary gonadotropin , CRH. Corticotropin-realising hormone Criminal behaviour, Klinefelter yndrome, Crinone. Micronized progesterone gel Crinophagy, Critical illness. Stress acute phase metabolic ponse , neuroendocrine response , versus response prolonged illness, adrenal function , biochemical monitoring , biphasic neuroendocrine response , catecholamines , chronic phase , metabolic response , Cushing syndrome , definition , endocrine therapeutics , euthyroid sick syndrome , glucagon , gonadal axis , gonadotropins , growth hormone , growth hormone therapy , hypercortisolism , prognostic significance , hyperglycemia , hypoadrenalism , hypogonadotropic hypogonadism , cytokines , hypomagnesemia , hypophosphatemia , hypotension , hypothalamic-pituitary-adrenal axis , biphasic response pattern , dysfunction , uitary-thyroid axis , immunologic response , immunomodulation , insulin , insulin , insulin-like growht factor-I , markers candidate, metabolic, mediators candidate, endocrine, metabolic response , ebb phase , flow phase , eral metabolities , neuroendocrine response , acute versus chronic phase, as beneficial adaptation versus dysfunction, biphasic, central, factors affecting, fuel lism, peripheral, stimuli , nutritional assessment , nutritional support , biochemical monitoring , oxygen free radicals , parathyroid hormone , pituitary , pressor support , prognosis , ionized calcium level , prolactin , prolonged, neuroendocrine response , versus response acute phase, protein administration , guidelines , protein catabolism , triiodothyronine therapy , renin-angiotensin-aldosterone system , severity , corrlation with plasma cortisol level, genitalsteroids , somatotropic axis , stress , systemic inflammation , terminal illness, comparison , testosterone levels , therapeutic considerations , thyroid axis , thyroid function parameters, vasodilation , vasopressin , vitamin D , wasting syndrome , androgen therapy , therapy , Critical period , brain development, Crix belly. HIV-associated fat redistribution Crk adapter proteins, IGF-I signaling pathway, Crohn disease (CD) atypical, clinical manifestations , confirmation diagnosis, prognosis , treatment , pregnancy , total parenteral nutrition, treatment , Cromolyn sodium effects endocrine function values, mast cell inhibition by, therapy with allergic rhinitis, mastocytosis, Crooke cells, CRO-related proteins, skiin, Crossing over, Cross talk, parathyroid hormone action, CRST syndrome (calcinosis, telangiectasia), ocular anifestations , Crude fiber, Cryptococcosis adrenal involvement , Cushing syndrome, adrenalitis caused by, central nervous system infection, hypercalcemia with, pancreatic involvement , thyroid involvement, raneoplastic ACTH syndrome, susceptibility , corticosteroids , thyroid abscess caused by, (INDEX - 2323) (INDEX -2324) Cryptrochidism, Testis / testes, undescended associated anomalies, causes , chromosomal anomalies , classfication , complications , definition , delayed puberty, diagnosis , effects fertility, embryology , history-taking , HLA association , hormonal therapy , hypogonadism, hypogonadotropic hypogonadism, hypospadias , incidence , infertility, laboratory findings with, malignant potential , physical findings , surgery , testicular endocrine function after, testicular atrophy with, testicular cancer, eatment , Cryptosporidium parvum, , pancreatic involvement , Crystalluria, with nephrolithiasis, Crystals Reinke, CSF. Cerebrospinal fluid; Colony-stimulating factor(s) CST. Cortistatin(s) CT. Computed tomography CT-1. Cardiotropin-1 CTAP. Connective tissue-activating peptide CT:CCP-I in:calcitonin carboxypeptide-I). Calcitonin, immature, conjoined with CCP-I peptide CTLA-4, secretion , islet transplant protection, CTNS gene, C-type natriuretic peptide. Natriuretic peptide(s), C-type Cumulative incidence, Cumulus adherens, Cumulus granulosa cells, expansion , Cunningham, Glenn R., Curare preparations, effects endocrine function values, Curettage amenorrhea after, dysfunctional, uterine bleeding, Curretab., Medroxyprogesterone acetate Cushing disease, Adreno-corticotropic hormone, hypersecretion ; Hyperadrenocorticism (Cushing disease, Cushing syndrome); Hypercortisolism ACTH secretion , adrenal cortex , adrenal surgery , anorexia nervosa , aseptic necrosis , cardiovascular disease risk , children, treatment , results , clinical manifestations , corticotrope hyperplasia , cortisol secretion , Crooke cells , cutaneous manifestations , definition , delayed puberty, dexamethasone suppression test , diagnosis , atypical confirmation , typical endocrine evaluation , growth failure , histopathology , hyperprolactinemia , imaging , infancy childhood, medical therapy , mental symptoms , ocular manifestations , osteopenia , otolaryngologic considerations , pathophysiology , petrosal sinus sampling , pituitary-dependent, pituitary lesions , detection , pituitary surgery , prognosis , prolactin secretion , radiation therapy , particle beam irradiation , stereotactic, radiosurgery , stereotactic, recurrence , after surgical treatment, delayed, serum osteocalcin levels , surgery , cure rate with, decision making , results , pediatric patients, treatment , Cushing syndrome, Adrenocorticotropic hormone, hypersecretion ; Hyperadrenocorticism (Cushing disease, Cushing syndrome); Hypercortisolism ACTH (corticotropin)-dependent, adrenal cortex , bilateral adrenal involvement , diagnosis , differential diagnosis , pathophysiology , pituitary. Cushing disease ACTH (corticotropin)-independent, adrenal cortex , bilateral adrenal involvement , causes , clinical manifestations , differential diagnosis , treatment , with ACTH-secreting gastrointestinal tumor, bone biposy , cardiovascular effects , cerebral effects , childhood osteopenia , chronic anovulation , classification , by etiology, clinical manifestations , critical illness, cutaneous manifestations , dental / orofacial abnormalities , diagnosis , confirmation , definitive, pregnancy, standard evaluation , differential diagnosis , CRH test , drug-induced, ectopic ACTH syndrome, clinical manifestations , elderly, endogenous, exogenous, hirsutism , hypertension , iatrogenic, alternate-day glucocorticoid therapy , , imaging , infancy childhood, diagnosis , infections , insulin resistance , laboratory findings , lipid tumors , localization cause , petrosal sinus sampling , medical therapy , neuromuscular manifestations , obesity , ocular manifestations , osteoporosis caused by, paraneoplastic syndromes, pathophysiology , pituitary-dependent differential diagnosis , plasma ACTH levels , pituitary-dependent differential diagnosis , plasma ACTH levels , pituitary-independent, differential diagnosis , plasma ACTH levels , Pneumocystic carinii prophylaxis , postprandial, pregnancy, diagnosis , fetal mortality rate with, treatment , prognosis , pseudo-Cushing syndrome, differentiation , radiosurgery , stereotactic, renal effects , respiratory effects , skiin , with somatostatinoma, surgical management , preoperative preparation patient , testicular failure, trace minerals, treatment , medical, pregnancy, triglyceride levels , Cutis verticis gyrata, CV 205-502. Quinagolide Cx37, oocyte growth, Cx43, 919 Cyanide, effects endocrine function values, Cyanide-nitroprousside test, amino-acid disorders, Cyclic adenosine monophosphate (cAMP), bone resorption, cellular content , histamine , extracellular, formation , gene transcription, glycogenolysis, hCG synthesis, intracellular level , hormones affecting, mast cell activation, metabolism , mRNA degradation, nephrogenous as bioassay PTH, humoral hypercalcemia malignancy, parathyroid hormone secretion, plasma / serum level , thyroid function , reference values , renal calcium handling, renin release, as second messenger, (INDEX-2325) steroidogenesis, urinary hormones affecting, as indicator PTH action, measurement , parathyroid hormone , prmary hyperparathyroidism, Cyclic adenosine monophosphate / protein kinase A pathway, genitalsteroid-binding hormone , Cyclic edema, Cyclic guanosine monophosphate (cGMP) endothelium, intrarenal actions , natriuretic peptide recptor signaling, penile crection, platelets, renin release, as second messenger, somatostatin gene expression, Cyclin DI IGF-I signaling pathway, pathyroid adenomas, Cyclo(His-Pro), central nervous system effects , Cyclobenzaprine, effects endocrine function values, Cyclofem, Cyclooxygenase, activity , critical illness, arachidonic acid metabolism, COX-1, critical illness, arachidonic acid metabolism, COX-1, implantation, COX-2, inhibitors , pancreatic islets, epidermis, inhibition , by aspirin, production , vasoconstriction, Cyclopentylpropionate. Testosterone cypionate, Cyclophosphamide effects endocrine function values, Graves opthalmopathy, endocrinologic side effects , indications , male hypogonadism, male intertility, vasopressin secretion , Cyclopia, Cyclopropane, effects endocrine function values, Cyclo-Provera, Cyclos erine, effects endocrine function values, Cyclosporine adverse effects side effects , aldosterone synthesis, cancer treatment, endocrine effects , effects endocrine function values, hypoaldosteronism caused by, mechanism action , nephrotoxicity , pathogenesis , plus prednisone, Graves ophthalmopathy, renal magnesium loss, therapy with Graves ophthalmopathy, pancreas transplant recipient, prevention type 1 A diabetes, type 1A diabetes, Cycrin. Medroxyprogesterone acetate CYP. Cytochrome P450 Cyproheptadine hydrochloride (Periactin), actions , adverse effects side effects , dosage administration , effects endocrine function values, indications , pharmacology , preparations , therapy with ACTH hypersecretion, children, eating disorders, idiopathic hyperaldosteronism, Nelson syndrome, Cyproterone acetate, Antihistamines chemical structure , effects endocrine function values, gynecomastia, as male contraceptive, male pseudohermaphroditism, therapy with acne, breast cancer, hirsutism, McCune-Albright syndrome, precocious puberty, prostate cancer, after relapse, Cyst(s) arachnoid, bone, renal osteodystrophy, branchial cleft, corneal, causes , epidermal inclusion, MEN1, follicular, luteal, ovarian.; Ovarian cyst(s) Rathke cleft. Rathke cleft cyst(s) renal, paraneoplastic syndromes with, theca lutein, thyroglossal duct, imaging , signs symptoms , thyroid clinical management , differential diagnosis , ultrasound , Cystathionase deficiency, cutaneous manifestations , ocular effects , organ-specific involvement , Cystathioninuria, Cysteine, structue , Cysticercosis (Cysticercus) pituitary involvement by, thyroid, Cystic fibrosis diabetes secondary , glucose intolerance , infertility, plasma / serum levels pulmonary hormones, preimplantation diagnosis , uniparental inheritance , vasoactive intestinal peptide abnormality inl Cystic fibrosis transmembrane conductance regulator, gene , Cystic hygroma, Cystine reference values , structure , Cystine knot, subunits glycoprotein hormones, Cystine screen, urinary, measurement , patient with nephorlithiasis, Cystine stones. Nephrolithiasis, cystine Cystinosis, benign (adult), late-onset, linkage analysis , nephropathic, ocular manifestations , ocular manifestations , organ-specific involvement , prenatal diagnosis , treatment , Cystinuria, organ-specific involvement , urine screening test , Cystitis, genital function, Cystosarcoma phylloides, Cystoscopy, nephrolithiasis, Cytadren. Aminoglutethimide Cytarabine, effects endocrine function values, Cytochrome oxidase, copper , Cytochrome P450, catalytic site , CYP1, CYP11, CYP11A (cholesterol desmolase), characteristics , deficiency , genetics , gene , mutations , steroidogenesis, CYP11B1 (11vita-hydroxylase), 11 Vita-Hydroxylase gene , mutations , CYP11B2 (aldosterone synthase), Aldosterone synthase gene (CYP11B2), mutations , CYP17 (17 alfa-hydroxylase / 17, 20-lyase), 17-alfa-Hydroxylase / 17, 20-lyase gene , mutations , male, pseudohermaphroditism, steroidogenesis, CYP19 (aromatase). Aromatase gene , mutations , mutations , delayed puberty, CYP 21 (21-hydroxylase), 21-Hydroxylase antibodies , gene CYP21P pseudogene, recombinations between, mutations , CYP24, CYP 27, CYP450 aldo. Cytochrome P450, CYP11B2 (aldosterone synthase) CYP 450c17, male pseudohermaphroditism, CYP450scc, Cytochrome P450, CYP11A antibodies , heme group , hepatic, inducers , endocrine side effects , , microsomal, mitochondrial, as mixed function oxidases, products, therapeutic potential , reductase, Cytogenetic map, Cytokeratin, thyroid, Cytokine(s), ACTH secretion, actions , administration , inflammatory effects , with alfa-helical structure, AIDS wasting syndrome, therapy directed at, amnionic fluid, angiogenic, antiangiogenic, antinflammatory, actions , administration , antiinflammatory effects , functions , production , antiviral, arachidonic acid metabolism, (INDEX-2326) Cytokine(s) (continued) autocrine effects , autoimmune hypothyroidism, autoimmune thyroiditis, bone metabolism, with vita-sheet structure, cell sources , cellular physiologic roles , central nervous system, chemotactic, clinical significance , critical illness, critical illness, chronic phase, C-type natriuretic peptide expression, definition , delection , effects growth development, embryologic growth differentiation, endocrine cell, endocrine effects , endocrine glands, endometriosis, eosinophils, feeding behaviour, functions , general features , glucocorticoids goiter, gonadal synthesis , Graves opthalmopathy, growth hormone secretion, chronic stress, growth modulatory, hematopoiesis, hemocrine effects , hormones, differences between, hurmoral hypercalcemia malignancy, hyperreninemic hypoaldosteronism ill patients, hypocalcemia, critical illness, hypothalamic-pituitary-adrenal axis, hypothalamic-pituitary axis, hypothalamic-pituitary-thyroid axis, immune functions , immune-mediated target cell damage, immunoregulatory, actions , cell sources , increased serum calcitonin precursors inflammation, infection, sepsis, inhibiotrs, AIDS wasting syndrome, islet transplant protection, leptin secretion, lipid metabolism abnormalities, , macrophage-derived, mast cell-derived, mechanism action , mimetics, therapeutic potential , with mutliple biologic responses, neonatal production , central nervous system effects , neuroimmunoendocrinology, neutralizing antibodies , overlapping actions , pancreas, paracrine effects , physicochemical characterisitcs , placental CRH output, plasma / serum level , models sepsis, pleiotropic, prevention cell death, production by blood cells, glucocorticoids , mast cells, by monocytes, regulation , by T cells, proinflammatory, actions , adipocytes, body protein erosion critical illness, cell sources , critical illness acute phase, acute versus chronic phase, chronic phase, gonadal effects , glucocorticoid resistance, hypothalamic-pituitary-thyroid axis, , mast cell-derived, secretion , by adipose tissue, sepsis, prostaglandin production fetal membrances, PTHrP PGE., linkage among, pulmonary, pharmacologic / physiologic effects , reciprocal inhibition by, redundancy , sepsis, pathogenic role , skeletal effects , skiin, sleep-promoting properties , somatostatin release, sources sympathetic nervous system, systemic effects , with therapeutic applications, thermoregulation, three-dimensional structure , thyroid-associated ophthalmopathy, thyroid hormone modulation nonthyroidal illness, thyroid-stimulating hormone secretion, as transmembrane proteins, trophoblastic, trypanosomiasis, type 1 diabetes, urinary excretion , Cytokine antagonist(s), Graves ophthalmopathy, Cytokine class 1 receptor superfamily, Cytokine receptor(s), cytoplasmic domain , deletion , effects growth development, downregulation , endocrine organs, hydrophobic region , recognition domain , soluble, urinary excretion , Cytomegalovirus (CMV) infection adrenalitis caused by adrenalitis caused by, central caused by, central nervous system involvement , hypercalcemia with, hypothalamic-pituitary involvement , pancreatic involvement , pituitary involvement , testicular involvement , pituitary involvement , subacute thyroiditis, susceptibility , corticosteroids , Cytomel. Liothyronine sodium Cytopenia, immune-mediated, corticosteroids , Cytoplasm, secretory cell, Cytoplasmic retinoic-acid-binding protein(s), type 1 (CRABP-1) HIV-associated fat redistribution, Cytosine arabinoside, male infertility, Cytoskeleton, preimplantation embryo, Cytotoxicity, definition , Cytotoxic therapy, hyperphosphatemia with, Cytotrophoblast, travillous, villous, D 1,25 (OH)2 D. 1,25-Dihydroxyvitamin D (1,25-dihydroxyvitamin D3) 1,25 (OH)2 D. 1,25-Dihydroxyvitamin D (1,25-dihydroxyvitamin D3) 2,4-D, toxic effects , 24,25 (OH)2 D.. 24,25-Dihydroxycholecalciferol 25(OH)D. 25-Hydroxyvitamin D 25(OH) D3. 25-Hydroxyvitamin D Dacarbazine effects endocrine function values, therapy with , endocrinologic side effects , insulinomas, Dactinomycin effects endocrine function values, testicular tumors, DAG. 

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