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Case Report

A Case of Moyamoya Disease with Neurofibromatosis Type I

Mi A Lee, Joo Pil Eum, Hae Young Lee, Byung Ho Cha

Clin Exp Pediatr. 2005;48(1):93-96. Published online January 15, 2005

Neurofibromatosis type I is an autosomal dominant disorder with varied manifestations in bone, soft tissue, the nervous system and skin. This is characterized by cafe-au-lait spots, neurofibromas, Lisch nodules, optic glioma, bony displasia, and intertriginous freckling. One of the more serious aspect of the disease relates to the arterial involvement. Vascular changes in neurofibromatosis may occur in any arterial tree...

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