Coat’s like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management options

BACKGROUND: Mutations in the CRB1 gene are associated with variable phenotypes of severe retinal dystrophies, and retinal dystrophies resulting from CRB1 mutations may be accompanied by specific fundus features such as coat’s like vasculopathy in retinitis pigmentosa patients. This is the first repo...

Descripción completa

Detalles Bibliográficos
Autores principales: Hasan, Somar M., Azmeh, Arwa, Mostafa, Osama, Megarbane, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752793/
https://www.ncbi.nlm.nih.gov/pubmed/26872607
http://dx.doi.org/10.1186/s13104-016-1917-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752793/
https://www.ncbi.nlm.nih.gov/pubmed/26872607
http://dx.doi.org/10.1186/s13104-016-1917-6

Ejemplares similares