Tag: "featured"

Pulmmer-Vinson Syndrome

Pulmmer-Vinson Syndrome

The triad of upper esophageal webs(small growth of tissue in esophagus) , dysphagia and iron deficiency anemia is called

Klinefelter Syndrome

Klinefelter Syndrome

Klinefelter syndrome is a genetic condition in which males have an one extra X sex chromosome characterized by male hypogonadism and infertility

Premature ovarian failure

Premature ovarian failure

Premature ovarian failure is the condition characterized by infertility, amenorrhea, hot flashes, night sweat, mood swings, irritability

Wilson’s Disease

Wilson’s Disease

It is a rare autosomal recessive disorder characterized by deposition of copper in the liver, brain and other organs due to increase absorption

Insulinoma

Insulinoma

Insulinoma is the beta cells tumor of the pancreas characterized by the signs and symptoms of hypoglycemia due to increased secretion of insulin.

Poland’s Syndrome

Poland’s Syndrome

Poland’s syndrome is a rare nonfamilial disease characterized by ipsilateral ( one sided) absence or underdeveloped chest wall muscles.

Hashimoto thyroiditis

Hashimoto thyroiditis

Hashimoto thyroditis is the autoimmune chronic inflammation of the thyroid gland leads to an underproduction thyroid hormones (hypothyroidism).

Sheehan syndrome

Sheehan syndrome

Sheehan syndrome also know as postpartum hypopituitarism, postpartum panhypopituitarism, postpartum panhypopituitary

Varicose veins

Varicose veins

Varicose veins is defined as tortuous dilated veins with dysfunction or nonfunctional valve. Varicose veins most commonly occurs in legs and feet

Mesothelioma

Mesothelioma

Mesothelioma is a rare neoplasm(tumor) of mesothelial cells lining the parietal and visceral pleura(protective layer that cover the many internal organs;such as lung

Pleurisy

Pleurisy

Pleurisy also called pleuritis is the inflammation of the pleura ( sac that cover the lungs which separates the lungs form chest wall,diaphragm and surrounding organs)

Crigler-Najjar syndrome

Crigler-Najjar syndrome

It is a rare autosomal recessive disorder affecting the metabolism of bilirubin results in jaundice in children and infants(usually first day of life)