GENERALIZED CHONDRODYSPLASIA PUNCTATA WITH SHORTNESS OF HUMERI AND BRACHYMETACARPY - HUMERO-METACARPAL (HM) TYPE - VARIATION OR HETEROGENEITY

被引:10
作者
BOROCHOWITZ, Z
机构
[1] S. Winter Ctr. for Human Gen., Bnai-Zion Medical Center, Box 4940
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 41卷 / 04期
关键词
CHONDRODYSPLASIA PUNCTATA; PUNCTATE EPIPHYSEAL CALCIFICATIONS; SHORT HUMERI; SHORT METACARPALS; SKELETAL DYSPLASIA;
D O I
10.1002/ajmg.1320410406
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a girl with symmetrical rhizomelic shortness of the upper limbs and punctate epiphyseal calcifications noted at birth. Presumably she has normal height, but short nose, short hands, and normal mentation; and on roentgenograms short and wide humeri, symmetrical brachymetacarpy, especially of the 4th metacarpals, and hypoplastic distal phalanges, sagittal clefting of vertebral bodies, and punctate calcifications at various areas including the entire spine, sacrum, hands, feet, trachea, and thyroid cartilage. It is an apparently new syndrome of chondrodysplasia punctata (CP), quite distinct from the classic form (Conradi-Hunermann type), as well as the other well-defined forms of CP. We thus suggest the term chondrodysplasia punctata, humero-metacarpal (HM) type.
引用
收藏
页码:417 / 422
页数:6
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