A case of bilateral Moyamoya disease associated with Williams syndrome

  • Hyung Suk Lee
  • , Dong Ick Shin
  • , Eun Ja Lee
  • , Sung Choon Park
  • , Sang Hoon Cha
  • , Jang Soo Hong
  • , Heon Seok Han
  • , Byeong Cheol Rim
  • , Sung Hyun Lee
  • , Sang Soo Lee

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Bilateral Moyamoya disease manifesting as ischemic stroke in a patient with Williams syndrome has not been previously reported. Williams syndrome is a genetic disorder characterized by infantile hypercalcemia, elfi n facial features, an outgoing personality, and cardiovascular abnormalities. It has been found to be related to elastin gene defect. Cerebrovascular abnormalities with associated strokes in Williams syndrome have been described only recently and rarely. Moyamoya disease is a cerebrovascular disorder characterized by progressive occlusion of the supraclinoid internal carotid artery. The pathogenesis of Moyamoya disease is unclear. Only a single report of Moyamoya disease associated with Williams syndrome manifesting as an intracerebral hemorrhage has been published. We report the fi rst case of bilateral Moyamoya disease manifesting as ischemic stroke in a patient with Williams syndrome. We propose that inherited moyamoya disease is also related to elastin gene defect.

Original languageEnglish
Pages (from-to)173-177
Number of pages5
JournalNeurology Asia
Volume15
Issue number2
StatePublished - Aug 2010

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