Neurofibromatosis type 1 associated with moyamoya syndrome. Case report and review of the literature.
Rom J Morphol Embryol
; 60(2): 713-716, 2019.
Article
em En
| MEDLINE
| ID: mdl-31658349
ABSTRACT
Neurofibromatosis type 1 (NF1) is a genetic disorder with a very heterogeneous clinical picture, affecting central nervous system, skin and bone system. Cerebrovascular lesions, such as moyamoya syndrome, are rarely seen in NF1. Approximately 250 children with NF1 and moyamoya syndrome have been reported. The clinical picture includes hemiparesis, hemianopsia, paresthesia, seizures, speech disorders, and intellectual disability. In this paper, we report on a 6-year-old girl with NF1 and moyamoya syndrome, with a brief review of the existing literature.
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Base de dados:
MEDLINE
Assunto principal:
Neurofibromatose 1
/
Doença de Moyamoya
Tipo de estudo:
Risk_factors_studies
Limite:
Child
/
Female
/
Humans
Idioma:
En
Ano de publicação:
2019
Tipo de documento:
Article