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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/8324


    Title: Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system
    Authors: Shaw, SW (Shaw, Sheng-Wen);Cheng, PJ (Cheng, Po-Jen);Chang, SD (Chang, Shuenn-Dhy);Lin, YT (Lin, Yu-Ting);Hung, CC (Hung, Chia-Cheng);Chen, CP (Chen, Chih-Ping);Su, YN (Su, Yi-Ning)
    Contributors: Department of Biotechnology
    Keywords: spinal muscular atrophy;prenatal diagnosis;DHPLC;QUANTITATIVE-ANALYSIS;SMN1 DELETION;COPY NUMBER;GENE;CARRIER;IDENTIFICATION;DOSAGE;PCR;SMA
    Date: 2008
    Issue Date: 2010-03-26 02:29:49 (UTC+0)
    Publisher: Asia University
    Abstract: Objective. Use of Denaturing High-Performance Liquid Chromatography (DHPLC) in prenatal diagnosis of spinal muscular atrophy (SMA). Methods. Thirty-three members of 7 families participated in carrier test and disease detection of SMA. Prenatal genetic diagnosis was performed if both parents were carriers or any family members had SMA. DNA extracted from blood, chorionic villi and amniotic fluid was amplified and used for DHPLC. Results. Twenty SMA carriers, seven SMA affected cases, and six normal individuals were identified. SMA status was demonstrated by genotyping and total copy number determinations of SMN1 and SMN2. Families 1-3 were classified as group one (SMA affecting previously born child). Group two, comprising families 4 and 5, had lost a child due to an unknown muscular disease. Group three (SMA-affected parent) comprised families 6 and 7; carrier testing was done. DHPLC prenatal genetic diagnosis was made in seven pregnancies, one in each family (affected, n = 2; carrier, n = 3; normal, n = 2). Pregnancy was terminated for the two affected fetuses. The others were delivered uneventfully and SMA free. Conclusion. DHPLC prenatal diagnosis of SMA and determination of SMA status in adults is possible, and SMN1 and SMN2 copy numbers can be determined.
    Relation: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA 87 (9): 960-968
    Appears in Collections:[生物科技學系] 期刊論文

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