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异常右锁骨下动脉导致产前诊断 Koolen-de Vries 综合征。

Aberrant right subclavian artery leading to prenatal diagnosis of Koolen de Vries syndrome.

机构信息

3rd Department of Obstetrics and Gynaecology, ATTIKON University Hospital Athens, Greece.

出版信息

Ginekol Pol. 2021;92(8):597-598. doi: 10.5603/GP.a2021.0157.

Abstract

Koolen de Vries syndrome is a rare genetic disorder with an estimated prevalence 1:16000 in the general population but it is considered to be an underdiagnosed syndrome. We report a 17q21.31 microdeletion which was diagnosed prenatally in a fetus with aberrant right subclavian artery (ARSA). Koolen de Vries syndrome is a rare chromosomal abnormality and according to the literature this is the first case in which the detection of ARSA led to this syndrome.

摘要

Koolen-de Vries 综合征是一种罕见的遗传性疾病,在普通人群中的患病率估计为 1:16000,但它被认为是一种未被充分诊断的综合征。我们报告了一例 17q21.31 微缺失,该缺失在一名胎儿中被诊断为右锁骨下动脉异常(ARSA)。Koolen-de Vries 综合征是一种罕见的染色体异常,根据文献记载,这是首例因检测到 ARSA 而导致该综合征的病例。

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