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

 

 

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 & VitaminD 

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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