HealthCareMagic is now Ask A Doctor - 24x7 | https://www.askadoctor24x7.com

Recently Updated Articles

Gilbert Disease

It is an herditary disease cause for increased bilirubin. It is an autosomal recessive condition charecterized by intermittent jaundice int he absence of hemolysis or liver disease.It is seen in 5% of the population.The main feature is that it causes jaundice which do not need treatment, caused by unconjugated bilirubin in the blood stream.
Read Full Article»
1288 Views

Anemia Congenital Pure Red Cell

Pure red cell aplasia (PRCA) describes a condition in which RBC precursors in bone marrow are nearly absent, while megakaryocytes and WBC precursors are usually present at normal levels. Pure red cell aplasia exists in several forms, and the most common form is an acute self-limited condition. Congenital pure red cell aplasia is a lifelong disorder, and it is associated with physical abnormalities. Acquired pure red cell aplasia is often chronic and is associated with underlying disorders such as thymomas and autoimmune diseases.
Read Full Article»
3807 Views

GHD (Growth hormone deficiency)

Growth hormone deficiency is a medical condition in which the body does not produce enough growth hormone. It is a disorder that involves pituitary gland which produces growth hormone. It affects all ages. It is treated by growth hormone therapy.
Read Full Article»
3508 Views

GHBP ( Growth hormone binding protein)

It is the carrier protein for growth hormone. It is coded by the gene which codes growth hormone receptor.It is decreased in genetic hormone insensitivity (Laron syndrome).
Read Full Article»
3541 Views

Alport Syndrome

Alport syndrome is a genetic disorder characterized by glomerulonephritis, end stage kidney disease, and hearing loss. Alport syndrome can also affect the eyes. The presence of blood in the urine (Hematuria) is almost always found in this condition.
Read Full Article»
2934 Views

Amyotrophic Lateral Sclerosis (ALS)

Amyotrophic Lateral Sclerosis (ALS) is a form of motor neuron disease which is progressive, fatal, neurodegenerative disease caused by the degeneration of motor neurons, the nerve cells in the central nervous system that control voluntary muscle movement resulting in progressive muscle wasting and atrophy.
Read Full Article»
1818 Views

Encopresis or Soiling or stool holding

It affects around 1% to 2% of kids under the age of 10. Most encopresis cases (90%) are due to functional constipation ? that is, constipation that has no medical cause. The stool (or BM) is hard, dry, and difficult to pass when a person is constipated. Many kids
Read Full Article»
4624 Views

Diet in peptic ulcer

A peptic ulcer is a sore area or erosion on the lining of the digestive system. If it is in the stomach it is called as gastric ulcer, if it is in the duodenum it is called duodenal ulcer.
Read Full Article»
3072 Views

Von Zambuschs Disease

Zambuschs disease or Von Zambuschs disease is also known as Csillag's Disease, Guttate Morphea, Guttate Scleroderma, Hallopeau I Disease, Lichen Sclerosus and White Spot Disease. It is a very uncommon condition which leads to patchy, white skin that's thinner than normal. It is a chronic inflammatory dermatosis that results in white plaques with epidermal atrophy. It mostly affects the genital like skin of the vulva, foreskin of the penis and anal areas. Sometimes, lichen sclerosus appears on the upper body, breasts, and upper arms.
Read Full Article»
3008 Views

Yunis Varon Syndrome

Yunis Varon syndrome is a rare and congenital disorder which involves multiple system malfunctions of the body. It generally affects the skeletal system, ectodermal system and sometimes the cardiorespiratory system is also suffered with various malfunctions.
Read Full Article»
1099 Views

 

« Previous 1 2 .... 83 84 85 .... 124 Next » Go to:
Browse Articles by category