Congenital hypertrophy of retinal pigment epithelium ; a polyposis registry experience

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...

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Veröffentlicht in:BMC research notes 2014-10, Vol.7
Hauptverfasser: Nusliha, Anwer, Dalpatadu, Ushantha, Amarasinghe, Binara, Chandrasinghe, Pramodh Chitral, Deen, Kemal Ismail
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Sprache:eng
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Zusammenfassung: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 easy to detect. This study found a high sensitivity and specificity for a CHRPE lesion to be associated with colonic polyps of FAP and hence a useful screening method in a burdened health-care system. The method is minimally invasive and simple and would be of particular value in screening children at risk for FAP.
ISSN:1756-0500
1756-0500
DOI:10.1186/1756-0500-7-734