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Cefalea en paciente con neurofibromatosis tipo 1

Herrero Valverde, A; Moiron Simões, R; Mera Campillo, J; Palma, T

INTRODUCTION: Neurofibromatosis type 1 (NF-1) is an autosomal dominant neurocutaneous syndrome due to a mutation in chromosome 17 (at 17q11.2). The association of NF-1 with Arnold-Chiari I malformation has been previously described. CASE REPORT: A 23 year-old woman diagnosed of NF-1 based on the presence of cutaneous lesions and a familiar background consistent with this was referred to the neurologist due to o...

Date: 2007   |   Origin: Repositório do Hospital Prof. Doutor Fernando Fonseca
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