孕早期胎儿双非整倍体核型48、XXY、+18 1例

Prenatal Cardiology Pub Date : 1900-01-01 DOI:10.12847/06144
L. Dudarewicz, U. Wysocka, L. Jakubowski
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引用次数: 0

摘要

摘要双非整倍体是一种罕见的现象,同时涉及18三体和Klinefelter综合征,其临床表现以Edwards综合征为主。我们描述了一个病人,谁被诊断在妊娠第8周与一个看似正常的宫内妊娠与“绒毛膜肿块”。第12周超声诊断如下异常:颈透明增加(4.7 mm),第四脑室前后径增大,第三脑室直径增大,心间质及心脏肥大。CVS核型为48、XXY、+18。我们认为,胎儿大脑第四脑室前后径增大可能是Dandy-Walker畸形的早期表现(由于妊娠早期终止而未得到证实),这是典型的爱德华兹综合征胎儿。我们认为妊娠早期胎儿第四脑室的前后直径增加是胎儿核型和进一步详细成像研究的指征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Double aneuploidy with karyotype 48,XXY,+18 in first trimester fetus - case report
Abstract Double anueploidy, involving both trisomy 18 and Klinefelter syndrome at the same time, is a rare event, in which the features of Edwards syndrome dominate the clinical picture. We describe a patient, who was diagnosed in the 8th gestational week with a seemingly normal intrauterine pregnancy with “chorionic bump”. In the 12th week the following abnormalities were diagnosed by ultrasound: Increased nuchal translucency (4.7 mm), increased anteroposterior diameter of the fourth ventricle and increased diameter of the third ventricle of the brain, mesocardia and cardiomegaly. The CVS karyotype revealed 48,XXY,+18 karyotype. In our opinion, the increased anteroposterior diameter of the fourth ventricle of the brain in this fetus was probably an early manifestation of the Dandy-Walker malformation (unproven because of early pregnancy termination), which is typical of Edwards syndrome fetuses. We consider the increased anteroposterior diameter of the fourth ventricle of the brain in the first trimester fetus as an indication for fetal karyotyping and further detailed imaging studies.
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