Clinical Polymorphism of Stargardt Disease in a Large Consanguineous Tunisian Family; Implications for Nosology

Purpose: To describe the polymorphic expression of Stargardt disease in a large Tunisian family with clinical intra- and interfamilial variation of the condition. Methods: Twelve subjects from two related families with autosomal recessive Stargardt disease were enrolled. A detailed clinical examina...

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Bibliographic Details
Main Authors: Leila El Matri, Farah Ouechtati, Ahmed Chebil, Leila Largueche, Sonia Abdelhak
Format: Article
Language:English
Published: Knowledge E 2013-01-01
Series:Journal of Ophthalmic & Vision Research
Subjects:
Online Access:http://www.jovr.org/article.asp?issn=2008-322X;year=2013;volume=8;issue=4;spage=341;epage=350;aulast=Matri