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[先天性发育缺陷儿童亲属的皮纹学研究]

[Dermatoglyphics of the relatives of children with congenital defects in development].

作者信息

Usoev S S

出版信息

Genetika. 1975;11(2):151-5.

PMID:131740
Abstract

The localization of an axial triradius and the flexor creases were studied in 173 phenotypically normal mothers and 104 fathers of congenitally malformed children. The most pronounced changes ofdermatoglyphics were found in the parents of children with polygenic determined defects, less pronounced ones-- in the parents of children with multiple congenital non-chromosomal defects and with Down's syndrome. The frequency of the pathological features studied was similar both in children with polygenically determined isolated defects and with Down's syndrome. The frequency of the pathological determined isolated defects and in their parents. In multiple congenital defects and in Down's syndrome the abnormalities ofof the localization of an axial triradius and of the flexor creases were found in children more frequently than in the parents. It is suggested that the above mentioned peculiarities of parental dermatoglyphics may be useful for the genetic counsleling.

摘要

对173名表型正常的母亲和104名先天性畸形儿童的父亲进行了轴三叉点和屈褶纹定位的研究。在多基因决定缺陷儿童的父母中发现皮纹最明显的变化,在患有多种先天性非染色体缺陷和唐氏综合征儿童的父母中变化较不明显。在多基因决定的孤立缺陷儿童和唐氏综合征儿童中,所研究的病理特征频率相似。在多基因决定的孤立缺陷及其父母中,病理特征的频率也是如此。在多种先天性缺陷和唐氏综合征中,儿童轴三叉点和屈褶纹定位异常的发生率高于父母。有人提出,父母皮纹的上述特点可能有助于遗传咨询。

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1
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