Stargadt’s disease in two Nigerian siblings

Stargardt’s disease is an inherited macular dystrophy that is transmitted in an autosomal recessive or dominant pattern. The disorder is typically characterized by impairment of central vision, with onset around the first 10–20 years of life. Stargardt’s disease is rare in sub-Saharan Africa. This i...

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Detalles Bibliográficos
Autores principales: Oluleye, Tunji S, Aina, Akinsola Sunday, Sarimiye, Tarela Frederick, Olaniyan, Segun Isaac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666157/
https://www.ncbi.nlm.nih.gov/pubmed/23750105
http://dx.doi.org/10.2147/IMCRJ.S38683

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666157/
https://www.ncbi.nlm.nih.gov/pubmed/23750105
http://dx.doi.org/10.2147/IMCRJ.S38683

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