3rd Department of Obstetrics and Gynaecology, ATTIKON University Hospital Athens, Greece.
Ginekol Pol. 2021;92(8):597-598. doi: 10.5603/GP.a2021.0157.
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.
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。