Ramesh K H, Verma R S
Division of Genetics, Long Island College Hospital, SUNY Health Science Center, Brooklyn 11201, USA.
Ann Genet. 1996;39(2):110-2.
Trisomy 18 (Edwards syndrome) is the second most common trisomy in human. The parental origin of the additional chromosome leading to meiotic errors is imperative to understand the etiology of trisomy 18. We compiled the data on 171 cases (table I) where meiotic error is provided. The paternal meiotic error occurred in 7% of the cases while in 93% of the cases nondisjunction took place in the mother. There were 28 cases (16%) where nondisjunction took place in meiosis I(MI), 53 cases (31%) in meiosis II (MII) and in 90 cases (53%) either the error was postzygotic mitosis or the dysfunctional stages could not be determined. The age distribution could be found in 119 cases (table II) and a conclusion could not be drawn as there were only 11 cases where paternal nondisjunction was noted.
18三体综合征(爱德华兹综合征)是人类中第二常见的三体综合征。导致减数分裂错误的额外染色体的亲本来源对于理解18三体综合征的病因至关重要。我们汇总了171例提供了减数分裂错误数据的病例(表I)。父源减数分裂错误发生在7%的病例中,而93%的病例中不分离发生在母亲身上。有28例(16%)不分离发生在减数分裂I(MI),53例(31%)发生在减数分裂II(MII),90例(53%)中错误要么是合子后有丝分裂,要么无法确定功能异常阶段。在119例病例中可以找到年龄分布情况(表II),由于仅记录到11例父源不分离病例,因此无法得出结论。