Moyamoya syndrome associated with neurofibromatosis type 1 in a pediatric patient

Moyamoya syndrome associated with neurofibromatosis type 1 in a pediatric patient

Abstract: 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, an...

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Bibliographic Details
Main Authors: Natália Battisti Serafini, Cássio Battisti Serafini, Alanna Santoro Vinhas, Marcio Barbosa Godinho
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2017-12-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Clinical diagnosis
Moyamoya disease
Neurofibromatosis 1
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962017000600870&tlng=en

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