Hereditas (Jul 2018)

A novel RASA1 mutation causing capillary malformation-arteriovenous malformation (CM-AVM): the first genetic clinical report in East Asia

  • Ren Cai,
  • Fatao Liu,
  • Chen Hua,
  • Zhang Yu,
  • Michele Ramien,
  • Claudia Malic,
  • Wenxin Yu,
  • Xiaolin Zhang,
  • Yun Liu,
  • Yunbo Jin,
  • Xun Hu,
  • Xiaoxi Lin

DOI
https://doi.org/10.1186/s41065-018-0062-8
Journal volume & issue
Vol. 155, no. 1
pp. 1 – 7

Abstract

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Abstract Capillary malformation-arteriovenous malformation (CM-AVM) is a clinical entity newly identified in 2003 that is caused by mutation of the RASA-1 gene, which encodes the protein p120-RasGAP. To date, most of the clinical reports on CM-AVM in the literature involve samples entirely consisting of Caucasians of European and North American descent, while reports from China or East Asia are few. Here, we describe a genetic clinical report of CM-AVM. Sequencing revealed a novel stop mutation in the RASA-1 gene causing loss of function (LOF) of the RasGAP domain. To our knowledge, this is the first genetic clinical report of a CM-AVM patient in East Asia. This report may extend our understanding and support further studies of CM-AVM in East Asia.

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