Prenatal diagnosis and genetic analysis of a fetus with endocardial cushion defects.
- VernacularTitle:一例心内膜垫缺损胎儿的产前诊断及遗传学分析
- Author:
Dong WU
1
,
2
;
Tao WANG
;
Qiaofang HOU
;
Tao LI
;
Xin WANG
;
Chaoyang ZHANG
;
Yanli YANG
;
Hongli LIU
;
Shixiu LIAO
Author Information
- Publication Type:Journal Article
- From: Chinese Journal of Medical Genetics 2018;35(3):418-421
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo perform prenatal diagnosis for a fetus with endocardial cushion defect and explore its mechanism.
METHODSThe karotypes of the fetus and its parents were analyzed by routine G-banding. Their genomic DNA was also analyzed by array comparative genomic hybridization (aCGH).
RESULTSThe fetus and its mother were found to have a karyotype of 46, XX, inv(8)(p21q24.1), while no karyotypic abnormality was detected for the father. aCGH has detected a 15.14 Mb deletion at 8p23.3-p22 and a 6.87 Mb duplication at 8q24.23-q24.3 in the fetus.
CONCLUSIONThe fetus was diagnosed with Rec8 syndrome. Its abnormal chromosomes have derived from the inv(8) carried by its mother. GATA4 and SOX7 may be the key genes for the endocardial cushion defect found in the fetus.
