Duarte A C, Cunha E, Roth J M, Ferreira F L S, Garcias G L, Martino-Roth M G
Serviço de Aconselhamento Genético, Departamento de Zoologia e Genética, Instituto de Biologia, Universidade Federal de Pelotas, Pelotas, RS, Brasil.
Genet Mol Res. 2004 Sep 30;3(3):303-8.
From 1986 to 2002, we examined the chromosomal composition of 916 patients attended by two genetic counseling services in the city of Pelotas, in the Brazilian State of Rio Grande do Sul, to determine the genetic causes of their disturbances. Patterns of G-banding using trypsin and Giemsa (GTG) and C-banding using barium and Giemsa (CBG) were studied using phytohemagglutinin M-stimulated lymphocytes cultured from peripheral blood. Among the patients, 110 had Down's syndrome, 7 had Edward's syndrome, 4 had Patau's syndrome, 29 had Turner's syndrome, 5 had Klinefelter's syndrome, and 3 had "cri-du-chat" syndrome. Abnormal chromosomes were observed in 29.3% of the patients. Most of these (56.3%) were numerical abnormalities, with the remaining being structural variants.
1986年至2002年期间,我们对巴西南里奥格兰德州佩洛塔斯市两家遗传咨询机构接待的916名患者的染色体组成进行了检查,以确定其病症的遗传原因。使用从外周血培养的植物血凝素M刺激的淋巴细胞,研究了用胰蛋白酶和吉姆萨染色的G显带模式(GTG)以及用钡和吉姆萨染色的C显带模式(CBG)。在这些患者中,110人患有唐氏综合征,7人患有爱德华兹综合征,4人患有帕陶氏综合征,29人患有特纳综合征,5人患有克兰费尔特综合征,3人患有“猫叫综合征”。29.3%的患者观察到染色体异常。其中大多数(56.3%)是数目异常,其余为结构变异。