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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Materias: | |
| 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 |