Twig-like middle cerebral artery in a case of neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with multisystemic involvement, affecting central nervous system, skin, bone system and vessels, with a very heterogeneous clinical presentation. Vascular abnormalities are typically recognized in neurofibromatosis type 1 affec...

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Detalles Bibliográficos
Autores principales: Orciulo, Grazia Vittoria, Grasso, Daniela, Borreggine, Carmela, Castorani, Giulia, Vergara, Doriana, Nasuto, Michelangelo, Ciccarese, Giovanni, Popolizio, Teresa, Serricchio, Ettore, Guglielmi, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510994/
https://www.ncbi.nlm.nih.gov/pubmed/36239750
http://dx.doi.org/10.23750/abm.v93iS1.13059
Descripción
Sumario:Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with multisystemic involvement, affecting central nervous system, skin, bone system and vessels, with a very heterogeneous clinical presentation. Vascular abnormalities are typically recognized in neurofibromatosis type 1 affecting cardiovascular and cerebrovascular systems. The incidence of circle of Willis anomalies in children with NF1 is twofold higher than in general population. In this paper, we report of 19-years-old female with NF1 and twig-like middle cerebral artery. (www.actabiomedica.it)

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