Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache

Sturge-Weber syndrome (SWS) is a congenital, sporadic, and rare neurocutaneous disorder, characterized by the presence of a facial port-wine birthmark (PWB), glaucoma, and neurological manifestations including leptomeningeal angiomatosis and seizures. It is caused by a postzygotic, somatic, gain-of-...

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Detalles Bibliográficos
Autores principales: Sánchez-Espino, Luis Fernando, Ivars, Marta, Antoñanzas, Javier, Baselga, Eulalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145477/
https://www.ncbi.nlm.nih.gov/pubmed/37124240
http://dx.doi.org/10.2147/TACG.S363685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145477/
https://www.ncbi.nlm.nih.gov/pubmed/37124240
http://dx.doi.org/10.2147/TACG.S363685

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