Miyazaki K, Yamanaka T, Ogasawara N
Department of Pediatrics, Central Hospital, Aichi, Japan.
Clin Genet. 1987 Dec;32(6):383-7. doi: 10.1111/j.1399-0004.1987.tb03154.x.
A 5-year-old boy with Down's syndrome of mild phenotype is described. Chromosome studies revealed that the karyotype of the proband was 46,XY,rec(21),dup q,inv(21) (p11.2q22.1)mat, and the segment 21q22.1----21qter was trisomic. The erythrocyte superoxide dismutase-1 (SOD-1) was found to be normal, and so we conclude that SOD-1 excess is not necessarily observed in patients with Down's syndrome caused by partial 21 trisomy. It is suggested that the gene for SOD-1 is located on the more proximal segment of the sub-band 21q22.1.
本文描述了一名具有轻度表型的5岁唐氏综合征男孩。染色体研究显示,先证者的核型为46,XY,rec(21),dup q,inv(21)(p11.2q22.1)mat,21q22.1----21qter片段三体。红细胞超氧化物歧化酶-1(SOD-1)正常,因此我们得出结论,部分21三体所致唐氏综合征患者不一定会出现SOD-1过量。提示SOD-1基因位于21q22.1亚带的更近端片段上。