Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations

To assess the progression of Stargardt (STGD) disease over nine years in two branches of a large consanguineous Tunisian family. Initially, different phenotypes were observed with clinical intra- and interfamilial variations. At presentation, four different retinal phenotypes were observed. In pheno...

Descripción completa

Detalles Bibliográficos
Autores principales: Falfoul, Yousra, Habibi, Imen, Turki, Ahmed, Chebil, Ahmed, Hassairi, Asma, Schorderet, Daniel F., El Matri, Leila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875050/
https://www.ncbi.nlm.nih.gov/pubmed/29736279
http://dx.doi.org/10.1155/2018/1030184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875050/
https://www.ncbi.nlm.nih.gov/pubmed/29736279
http://dx.doi.org/10.1155/2018/1030184

Ejemplares similares