Ocular Manifestations of the Sturge–Weber Syndrome

Abstract 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...

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Bibliographic Details
Main Authors: Kiana Hassanpour, Ramin Nourinia, Ebrahim Gerami, Ghavam Mahmoudi, Hamed Esfandiari
Format: Article
Language:English
Published: Knowledge E 2021-07-01
Series:Journal of Ophthalmic & Vision Research
Subjects:
Online Access:https://doi.org/10.18502/jovr.v16i3.9438