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Moyamoya syndrome and neurofibromatosis type 1

Authors :
Evdoxia Sapountzi
M. Kyriazi
Dimitrios I. Zafeiriou
Athanasia Anastasiou
Dimitris Samakovitis
Euthymia Vargiami
Spyros Batzios
Source :
Italian Journal of Pediatrics
Publisher :
Springer Nature

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.

Details

Language :
English
ISSN :
18247288
Volume :
40
Issue :
1
Database :
OpenAIRE
Journal :
Italian Journal of Pediatrics
Accession number :
edsair.doi.dedup.....a75b5f6348413e3858779c177b2f6499
Full Text :
https://doi.org/10.1186/1824-7288-40-59