Moyamoya syndrome and neurofibromatosis type 1 View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2014-06-21

AUTHORS

Euthymia Vargiami, Evdoxia Sapountzi, Dimitris Samakovitis, Spyros Batzios, Maria Kyriazi, Athanasia Anastasiou, Dimitrios I Zafeiriou

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. More... »

PAGES

59

Identifiers

URI

http://scigraph.springernature.com/pub.10.1186/1824-7288-40-59

DOI

http://dx.doi.org/10.1186/1824-7288-40-59

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1048592937

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24952383


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178 schema:name 1st Department of Pediatrics, Aristotle University of Thessaloniki, Egnatia St. 106, 54622, Thessaloniki, Greece
179 rdf:type schema:Organization
 




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