Moyamoya syndrome and 6p chromosome rearrangements: Expanding evidences of a new association
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- 作者：Irene Toldoa ; irene.toldo@unipd.it" class="auth_mail" title="E-mail the corresponding author ; Chiara Po'a ; c_p0505@yahoo.it" class="auth_mail" title="E-mail the corresponding author ; Veronica Moraoa ; veronica85mo@libero.it" class="auth_mail" title="E-mail the corresponding author ; Giacomo Talentib ; giacomo.talenti@fastwebnet.com" class="auth_mail" title="E-mail the corresponding author ; Francesco Causinb ; francesco.causin@sanita.padova.it" class="auth_mail" title="E-mail the corresponding author ; Domenico D'Avellac ; domenico.davella@unipd.it" class="auth_mail" title="E-mail the corresponding author ; Romano Tenconid ; romano.tenconi@unipd.it" class="auth_mail" title="E-mail the corresponding author ; Agnese Suppieja ; suppiej@pediatria.unipd.it" class="auth_mail" title="E-mail the corresponding author ; Stefano Sartoria ; stefano.sartori@unipd.it" class="auth_mail" title="E-mail the corresponding author
- 关键词：Moyamoya syndrome ; Pediatric stroke ; Transient ischemic attack ; Chromosome rearrangement ; Short arm chromosome 6
- 刊名：European Journal of Paediatric Neurology
- 出版年：2016
- 出版时间：September 2016
- 年：2016
- 卷：20
- 期：5
- 页码：766-771
- 全文大小：371 K
文摘
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6p genomic region rearrangements can be associated with moyamoya angiopathy.
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6p region becomes a candidate genetic locus for cerebral vasculopathies.
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Brain magnetic angiogram is suggested in individuals carrying 6p rearrangements.
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CGH-array could be considered in patients with otherwise unexplained moyamoya.