Discovery of asymptomatic moyamoya arteriopathy in pediatric syndromic populations: radiographic and clinical progression.

@article{Lin2011DiscoveryOA,
  title={Discovery of asymptomatic moyamoya arteriopathy in pediatric syndromic populations: radiographic and clinical progression.},
  author={Ning Lin and Lissa Catherine Baird and McKenzie Koss and Kimberly E. Kopecky and Evelyne Gon{\'e} and Nicole N J Ullrich and Robert Michael Scott and Edward R Smith},
  journal={Neurosurgical focus},
  year={2011},
  volume={31 6},
  pages={E6}
}
OBJECT Limited data exist to guide management of incidentally discovered pediatric moyamoya. Best exemplified in the setting of unilateral moyamoya, in which the unaffected side is monitored, this phenomenon also occurs in populations undergoing routine surveillance of the cerebral vasculature for other conditions, such as sickle cell disease (SCD) or neurofibromatosis Type 1 (NF1). The authors present their experience with specific syndromic moyamoya populations to better characterize the… CONTINUE READING
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