Multiple retinal astrocytic hamartomas in siblings with lebers congenital amaurosis: a case series and review of literature

BACKGROUND: Leber’s congenital amaurosis (LCA) is a known inherited retinal disease (IRD) associated with severe visual loss, nystagmus, amaurotic pupils, oculo-digital sign and markedly reduced or absent electroretinograms (ERG). Retinal astrocytic hamartomas (RAH) is a benign vascularized glial tu...

Descripción completa

Detalles Bibliográficos
Autores principales: Paul, Lagan, Kumar, Sumit, Singh, Shalini, Jain, Tanya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510068/
https://www.ncbi.nlm.nih.gov/pubmed/32967644
http://dx.doi.org/10.1186/s12886-020-01646-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510068/
https://www.ncbi.nlm.nih.gov/pubmed/32967644
http://dx.doi.org/10.1186/s12886-020-01646-z

Ejemplares similares