Chondrodysplasia punctata, humero-metacarpal type: A second case

被引:0
|
作者
Fryburg, JS
Kelly, TE
机构
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 64卷 / 03期
关键词
chondrodysplasia punctata; punctate epiphyseal calcifications; rhizomelic shortening; short humeri; short metacarpals; skeletal dysplasia;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a boy with symmetrical rhizomelic shortness of the upper limbs and punctate epiphyseal calcifications noted at birth, Radiographs documented short and wide humeri, symmetrical brachymetacarpy, coronal clefts of the veretebrae, and punctate calcifications in the spine, sacrum, shoulder, feet, and trachea. Borochowitz [1991] described a similar patient with an apparently new syndrome of chondrodysplasia punctata (CP), distinct from previously described forms, He suggested the term ''chondrodysplasia punctata, humero-metacarpal (HM)'' type, We present our patient as a second case of this form of CP. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:493 / 496
页数:4
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