Ocular Manifestations of the Sturge–Weber Syndrome

Sturge–Weber syndrome (SWS) or encephalotrigeminal angiomatosis is a non-inherited congenital disorder characterized by neurologic, skin, and ocular abnormalities. A somatic activating mutation (R183Q) in the GNAQ gene during early embryogenesis has been recently recognized as the etiology of vascul...

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Detalles Bibliográficos
Autores principales: Hassanpour, Kiana, Nourinia, Ramin, Gerami, Ebrahim, Mahmoudi, Ghavam, Esfandiari, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PUBLISHED BY KNOWLEDGE E 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358762/
https://www.ncbi.nlm.nih.gov/pubmed/34394871
http://dx.doi.org/10.18502/jovr.v16i3.9438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358762/
https://www.ncbi.nlm.nih.gov/pubmed/34394871
http://dx.doi.org/10.18502/jovr.v16i3.9438

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