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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Hlavní autoři:	Natália Battisti Serafini, Cássio Battisti Serafini, Alanna Santoro Vinhas, Marcio Barbosa Godinho
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Sociedade Brasileira de Dermatologia 2017-12-01
Edice:	Anais Brasileiros de Dermatologia
Témata:	Clinical diagnosis Moyamoya disease Neurofibromatosis 1
On-line přístup:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962017000600870&tlng=en
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