Cargando…
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...
| Autores principales: | , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
PUBLISHED BY KNOWLEDGE E
2021
|
| Materias: | |
| 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 |