Cerebral Vasculopathy in Children with Neurofibromatosis Type 1

SIMPLE SUMMARY: Neurofibromatosis type 1 is a common autosomal dominant inherited condition, with variable phenotype among affected individuals. Abnormalities of the cerebral vasculature are an acknowledged but poorly understood complication, leading to high morbidity and mortality for individuals w...

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Detalles Bibliográficos
Autores principales: Lehman, Laura L., Ullrich, Nicole J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605225/
https://www.ncbi.nlm.nih.gov/pubmed/37894478
http://dx.doi.org/10.3390/cancers15205111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605225/
https://www.ncbi.nlm.nih.gov/pubmed/37894478
http://dx.doi.org/10.3390/cancers15205111

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