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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Knowledge E
2021-07-01
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Series: | Journal of Ophthalmic & Vision Research |
Subjects: | |
Online Access: | https://doi.org/10.18502/jovr.v16i3.9438 |