Li Dongzhi, Liao Can, Li Jian, Huang Yining, Xie Xingmei, Wei Jiaxue, Wu Shaoqing
Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China.
Hemoglobin. 2006;30(3):365-70. doi: 10.1080/03630260600755625.
Beta-thalassemia (thal) is the most common genetic disease and is widely distributed in southern China. Prenatal diagnosis is needed to prevent the birth of thalassemic offspring in couples at-risk. This can be performed in the first or second trimester of pregnancy by DNA analysis using polymerase chain reaction (PCR). As there are more than 30 mutations causing beta-thal in Chinese, the point mutation detection by reverse dot-blot for common mutations together with direct DNA sequencing was developed for prenatal diagnosis. Using reverse dot-blot, we were able to offer complete diagnosis in 315 (99.4%) of 317 pregnancies. Only two fetuses needed the DNA sequencing technique for diagnosis. Of the 319 at-risk fetuses, 82 (25.7%) were found to be normal, 143 (44.8%) to be heterozygous for beta-thal and 94 (29.5%) to be affected with beta-thal. Therefore, the combination of reverse dot-blot with direct DNA sequencing can perform prenatal diagnosis by DNA analysis in almost all cases at- risk of beta-thal in southern China.
β地中海贫血是最常见的遗传性疾病,在中国南方广泛分布。对于有风险的夫妇,需要进行产前诊断以防止地中海贫血患儿的出生。这可以在妊娠的第一或第二孕期通过使用聚合酶链反应(PCR)进行DNA分析来实现。由于在中国有30多种导致β地中海贫血的突变,因此开发了用于常见突变的反向点杂交点突变检测以及直接DNA测序用于产前诊断。使用反向点杂交,我们能够在317例妊娠中的315例(99.4%)中提供完整诊断。仅2例胎儿需要DNA测序技术进行诊断。在319例有风险的胎儿中,82例(25.7%)被发现正常,143例(44.8%)为β地中海贫血杂合子,94例(29.5%)患有β地中海贫血。因此,反向点杂交与直接DNA测序相结合几乎可以对中国南方所有有β地中海贫血风险的病例进行DNA分析产前诊断。