Binara Amarasinghe

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Familial Adenomatous Polyposis (FAP) is an autosomal dominant condition giving rise to multiple adenomatous polyps in the colon which invariably become malignant by the fourth decade. Congenital hypertrophy of retinal pigment epithelium (CHRPE) is one of its extra intestinal manifestations early in childhood seen, present in 90% of FAP population and is(More)
OBJECTIVES To improve the prognosis of patients with familial adenomatous polyposis (FAP) by early diagnosis and prophylactic treatment through a coordinated FAP register. DESIGN The establishment and descriptive analysis of the prospective database of the FAP registry. SETTING University surgical unit, Colombo North Teaching Hospital Ragama, Sri Lanka.(More)
Case reports appearance. Colonies grow rapidly and are flat, cream coloured and become radially folded covered by a fine powdery white surface consisting of mycelium and condiospores. Tan coloured colonies become brown with age [7]. Treatment consists of a combination of three or more drugs and surgery. KI, amphoteracine B, ketaconazole and itraconazole(More)
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