Health Articles (Sorted by date)
Complete Information on Cowden's disease
Cowden disease (CD), also known multiple hamartoma syndrome. It is an autosomal dominant condition with variable expression that results most commonly (80%) from a mutation in the PTEN gene on arm 10q, as reported by Liaw et al.
Abraham GalvinJuly 04, 2008
Complete Information on Cor triatriatum
Cor triatriatum is an inborn eye flaw where the left atrium is subdivided. The membrane divides the correct atrium into a proximal (upper) and a distal (lower) bedroom.
Abraham GalvinJuly 04, 2008
Complete Information on Conn's syndrome
The Conn comprehensive symptom is the adrenal gland gland disease involves the hormone overproduction. The adrenal gland gland is located above two kidneys the orange decadent internal secretion gland.
Abraham GalvinJuly 04, 2008
Complete Information on Congenital hepatic fibrosis (CHF)
Congenital hepatic fibrosis (CHF) is an uncommon genetic disorder characterized by periportal fibrosis with irregularly shaped proliferating bile ducts, intrahepatic portal hypertension, and esophageal varices.
Abraham GalvinJuly 04, 2008
Complete Information on Congenital diaphragmatic hernia
Congenital diaphragmatic hernia (too known as CDH) is an irregularity that occurs before birth as a fetus is forming in the mother's womb. Newborns with CDH frequently have serious respiratory distress which can be severe unless treated...
Abraham GalvinJuly 04, 2008
Complete Information on Cytomegalovirus
Cytomegalovirus (CMV) is a virus that infects most people worldwide. People are usually infected by the time they are 2 years old or during their teenage years.
Abraham GalvinJuly 04, 2008
Complete Information on Congenital amputation
Congenital amputation is an inborn disorder caused by fibrous bands of the amnion. This circumstance may be the outcome of the constriction of fibrous bands within the membrane that surrounds the developing fetus or the vulnerability to substances...
Abraham GalvinJuly 04, 2008
Complete Information on Congenital adrenal hyperplasia
CAH is a genetic defect of the adrenal glands. People with this condition do no produce enough of the hormones cortisol and aldosterone, and produce too much of androgen. It affects both males and females.
Abraham GalvinJuly 04, 2008
Complete Information on Cone rod dystrophy
Cone-Rod Dystrophy (CRD) is an inherited liberal disease that causes worsening of the cone and pole photoreceptor cells and frequently results in blindness.
Abraham GalvinJuly 04, 2008
Complete Information on Condyloma
Condlyoma is also known wart, genital wart and caused by a virus called the human papilloma virus. The virus is spread by skin-to-skin contact during activity and there does not need to be anal penetration in order to become infected.
Abraham GalvinJuly 04, 2008
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