Cardiology Division, Department of Human Genetics and Eccles Program in Human Molecular Biology and Genetics, University of Utah, Salt Lake City, UT 84112, USA.
Trends Cardiovasc Med. 1994 Jul-Aug;4(4):165-9. doi: 10.1016/1050-1738(94)90053-1.
Supravalvular aortic stenosis (SVAS) is a vascular disease that primarily affects large arteries, like the aorta and pulmonary arteries. SVAS can be inherited as an isolated, autosomal dominant trait or as part of a complex developmental disorder, Williams syndrome. Molecular genetic studies indicate that mutations affecting part of an elastin allele cause autosomal dominant SVAS while submicroscopic deletions that disrupt the entire elastin gene (and presumably adjacent loci) are responsible for Williams syndrome. These studies suggest that loss of vascular elasticity from any cause may contribute to vascular obstruction.
主动脉瓣上狭窄(SVAS)是一种主要影响大动脉的血管疾病,如主动脉和肺动脉。SVAS 可以作为一个孤立的、常染色体显性遗传特征遗传,也可以作为复杂发育障碍威廉姆斯综合征的一部分。分子遗传学研究表明,影响弹性蛋白等位基因一部分的突变导致常染色体显性 SVAS,而破坏整个弹性蛋白基因(和可能相邻的基因座)的亚显微缺失导致威廉姆斯综合征。这些研究表明,任何原因导致的血管弹性丧失都可能导致血管阻塞。