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    题名: Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15
    作者: 陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Chern, Schu-Rern;Wu, Peih-Shan;Ch, Shun-Ping;Kuo, Yu-Ling;Chen, Wen-Lin;Wang, Wayseen
    贡献者: 生物科技學系
    关键词: Amniocentesis;CES;Cat eye syndrome;DGS;DiGeorge syndrome;FISH;IUGR;LCR;MLPA;Mosaicism;OMIM;Online Mendelian Inheritance in Man;Prenatal diagnosis;Small supernumerary marker chromosome 22;TAPVR;VCFS;aCGH;array comparative genomic hybridization;cat eye syndrome;fluorescence in situ hybridization;intrauterine growth restriction;inv dup;inverted duplication;low-copy repeats;mar;marker chromosome;multiplex ligation-dependent probe amplification;sSMC;sSMC(22);small supernumerary marker chromosome;total anomalous pulmonary venous return;velocardiofacial syndrome
    日期: 2014-03
    上传时间: 2014-06-04 10:21:20 (UTC+8)
    摘要: We present prenatal diagnosis of mosaicism for a small supernumerary marker chromosome (sSMC) derived from chromosome 22 associated with cat eye syndrome (CES) using cultured amniocytes in a pregnancy with fetal microcephaly, intrauterine growth restriction, left renal hypoplasia, total anomalous pulmonary venous return with dominant right heart and right ear deformity. The sSMC was bisatellited and dicentric, and was characterized by multiplex ligation-dependent probe amplification (MLPA) and array comparative genomic hybridization (aCGH). The SALSA MLPA P250-B1 DiGeorge Probemix showed duplication of gene dosage in the CES region. aCGH showed a 1.26-Mb duplication at 22q11.1-q11.21 encompassing CECR1-CECR7. The sSMC was likely inv dup(22) (q11.21). Prenatal diagnosis of an sSMC(22) at amniocentesis should alert CES. MLPA, aCGH and fetal ultrasound are useful for rapid diagnosis of CES in case of prenatally detected sSMC(22).
    關聯: Taiwanese Journal of Obstetrics & Gynecology, 527(1):384-388.
    显示于类别:[生物科技學系] 期刊論文


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