AUTOSOMAL IMBALANCE SYNDROMES - GENETIC INTERACTIONS AND THE ORIGIN OF CONGENITAL-MALFORMATIONS IN ANEUPLOIDY SYNDROMES

被引:16
|
作者
LURIE, IW
机构
[1] Division of Human Genetics, Baltimore, MD 21201-1703
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 03期
关键词
AUTOSOMAL IMBALANCE SYNDROMES; DELETION-3P; DELETION-7Q; HOLOPROSENCEPHALY; POLYDACTYLY;
D O I
10.1002/ajmg.1320470323
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In some autosomal imbalance syndromes an additional imbalance interferes with the occurrence of the anomalies typical of the syndrome itself. For example, polydactyly was found in patients with ''pure'' del(3p) more frequently (11/23) than in patients where these deletions were associated with different partial trisomies (2/28). The opposite situation was shown in del(7q) syndrome where various defects of the holoprosencephalic group were found to be rarer in patients with ''pure'' deletions, than in cases with simultaneous occurrence of various partial trisomies. It suggests the importance of gene interaction in determining the phenotypic picture of autosomal imbalance syndromes. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:410 / 416
页数:7
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