Moyamoya syndrome associated with neurofibromatosis type 1 in a pediatric patient

• Main Authors: Natália Battisti Serafini (Author), Cássio Battisti Serafini (Author), Alanna Santoro Vinhas (Author), Marcio Barbosa Godinho (Author)
• Format: Book
• Published: Sociedade Brasileira de Dermatologia, 2017-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...