Abstract
Neurofibromatosis type 1 (NF1) is the most prevalent autosomal dominant genetic disorder among humans. NF1 vasculopathy is a significant but underrecognized complication of the disease, affecting both arterial and venous blood vessels of all sizes. Moyamoya syndrome is a cerebral vasculopathy that is only rarely observed in association with NF1, particularly in the pediatric age range. Herein, we report of a 5-year-old female with NF1 and moyamoya syndrome and we briefly review the existing literature. © 2014 Vargiami et al.; licensee BioMed Central Ltd.
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Vargiami, E., Sapountzi, E., Samakovitis, D., Batzios, S., Kyriazi, M., Anastasiou, A., & Zafeiriou, D. I. (2014, June 21). Moyamoya syndrome and neurofibromatosis type 1. Italian Journal of Pediatrics. BioMed Central Ltd. https://doi.org/10.1186/1824-7288-40-59
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