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Author

M. Amaral

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Review Open access Oct 2026

Headache in neurofibromatosis type 1: a systematic review

Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder caused by mutations in the NF1 gene on chromosome 17. This gene encodes neurofibromin, a key protein in the regulation of cell proliferation. With an estimated incidence of 1 in 3,000 live births, NF1 presents a heterogeneous cl...

Júlia Coutinho Cordeiro, M. Amaral, Gabriela Lavínia Santos Silva et al. · 0 citations

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