Kim Joong-Seok, Lee Kwang-Soo, Kim Yeong-In, Lee Kwon-Haeng, Kim Hong-Tae
Department of Neurology, Kangnam St. Mary Hospital, Catholic University of Korea, #505 Banpo-dong, Seocho-gu, Seoul 137-701, Korea.
Yonsei Med J. 2003 Apr 30;44(2):336-9. doi: 10.3349/ymj.2003.44.2.336.
The gene responsible for autosomal recessive parkinsonism, parkin, has recently been identified on chromosome 6q. It has been shown to be mutated in Japanese and European families, most of whom had early-onset parkinsonism. Here, we present a family with young-onset parkinsonism of an autosomal recessive inheritance. A homozygous exon 4 deletion in the parkin gene was found in 3 family members. To the best of the authors' knowledge, this is the first report in Korea of familial parkinsonism with the parkin gene mutation.
导致常染色体隐性帕金森症的基因——帕金蛋白基因,最近已在6号染色体长臂上被确认。在日本和欧洲的家族中已证实该基因发生了突变,其中大多数家族成员患有早发性帕金森症。在此,我们展示一个常染色体隐性遗传的早发性帕金森症家族。在3名家族成员中发现了帕金蛋白基因外显子4的纯合缺失。据作者所知,这是韩国首例关于帕金基因突变所致家族性帕金森症的报告。