[an error occurred while processing this directive]

HEREDITAS ›› 2009, Vol. 31 ›› Issue (6): 605-610.doi: 10.3724/SP.J.1005.2009.00605

• 研究报告 • Previous Articles     Next Articles

Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region

TAN Jian-Qiang1;WANG Ping2;HU Qi-Ping1;LI Song-Feng1;SHU Wei1;MA Jun1;FANG Ling1;HUA Rong1;DING Ye1;YUAN Zhi-Gang1   

  1. 1. Guangxi Medical University, Nanning 530021, China;
    2. Guangxi Zhuang Autonomous Region Public Security Bureau, Nanning 530000, China
  • Received:2008-11-30 Revised:2009-01-18 Online:2009-06-10 Published:2009-06-10
  • Contact: YUAN Zhi-Gang

Abstract: To characterize the distributions and subtypes of the spinocerebellar ataxias (SCA) in Guangxi region, the SCAl, SCA2, SCA3/MJD, SCA6, SCA7 and SCA12 (CAG)n mutations were analyzed by polymerase chain reaction (PCR) and capillary electrophoresis (CE). The SCA3/MJD mutation was detected in a total of 21 SCA patients and 19 presymptomatic individuals from 6 SCA families and their CAG repeat numbers were 59~70 and 60~73, respectively. No (CAG)n mutations of SCA1, SCA2, SCA6, SCA7 and SCA12 were detected. This study showed that SCA in Guangxi region is mostly SCA3/MJD subtype and the CAG repeats are smaller than those reported in other regions previously.