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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-...
Autores principales: | Sánchez-Espino, Luis Fernando, Ivars, Marta, Antoñanzas, Javier, Baselga, Eulalia |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Materias: | |
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 |
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