LANGER TYPE OF MESOMELIC DWARFISM AS THE POSSIBLE HOMOZYGOUS EXPRESSION OF DYSCHONDROSTEOSIS

被引：19

作者：

FRYNS, JP

VANDENBERGHE, H

机构：

[1] Division of Human Genetics, Department of Human Biology, Leuven, B-3000, Minderbroedersstraat

来源：

HUMAN GENETICS | 1979年 / 46卷 / 01期

关键词：

D O I：

10.1007/BF00278898

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A male newborn with the typical Langer type of mesomelic dwarfism is presented. The finding of a variable degree of Madelung's deformity and mesomelic shortening in both parents and in the maternal family tends to support the hypothesis that this type of mesomelic dwarfism may be the clinical manifestation of a homozygous state for dyschondrosteosis. © 1979 Springer-Verlag.

引用

页码：21 / 27

页数：7

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