Sturge–Weber Syndrome with Bilateral Port-Wine Stain

Sturge–Weber syndrome is a rare congenital neurocutaneous disorder characterized by dermatological, ophthalmological, and neurological manifestations. It occurs due to abnormal persistence of embryonic vascular plexus. Here, we describe a case of four years seven months female with seizures, develop...

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Detalles Bibliográficos
Autores principales: Pathak, Bishnu Deep, Sharma, Shriya, Adhikari, Aakriti, Simkhada, Nabin, Ghimire, Bhuwan, Aryal, Nirjala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033375/
https://www.ncbi.nlm.nih.gov/pubmed/35464665
http://dx.doi.org/10.1155/2022/2191465

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033375/
https://www.ncbi.nlm.nih.gov/pubmed/35464665
http://dx.doi.org/10.1155/2022/2191465

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