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
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
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