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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Detalles Bibliográficos
Autores principales: Serafini, Natália Battisti, Serafini, Cássio Battisti, Vinhas, Alanna Santoro, Godinho, Marcio Barbosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786411/
https://www.ncbi.nlm.nih.gov/pubmed/29364453
http://dx.doi.org/10.1590/abd1806-4841.20176829

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786411/
https://www.ncbi.nlm.nih.gov/pubmed/29364453
http://dx.doi.org/10.1590/abd1806-4841.20176829

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