Epidermal nevus syndrome with the mutation of PTCH1 gene and cerebral infarction: a case report and review of the literature

BACKGROUND: Epidermal nevus syndrome is a group of congenital neuroectodermal and/or mesodermal disorders characterized by the epidermal nevi in common association with cerebral, eye, skeletal, cardiovascular, and renal abnormalities. Epidermal nevus syndrome is a rare syndrome, and epidermal nevus...

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Detalles Bibliográficos
Autores principales: Deng, QingQing, Li, Yan, Liu, ZhanLi, Zhou, JieLin, Weng, LingWei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520847/
https://www.ncbi.nlm.nih.gov/pubmed/36171624
http://dx.doi.org/10.1186/s13256-022-03547-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520847/
https://www.ncbi.nlm.nih.gov/pubmed/36171624
http://dx.doi.org/10.1186/s13256-022-03547-9

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