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Moyamoya syndrome associated with neurofibromatosis type 1 in a pediatric patient
Neurofibromatosis type 1 is a multisystem genetic disease of autosomal dominant transmission that reveals important cutaneous manifestations such as café-au-lait spots, multiple neurofibromas, and ephelides in skin fold areas, as well as hamartomatous lesions in the eyes, bones, glands, and central...
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| Publicado no: | An Bras Dermatol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Sociedade Brasileira de Dermatologia
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5786411/ https://ncbi.nlm.nih.gov/pubmed/29364453 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20176829 |
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