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Chondrodysplasia punctata, humero-metacarpal type: a second case.

Authors :
Fryburg JS
Kelly TE
Source :
American journal of medical genetics [Am J Med Genet] 1996 Aug 23; Vol. 64 (3), pp. 493-6.
Publication Year :
1996

Abstract

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.

Details

Language :
English
ISSN :
0148-7299
Volume :
64
Issue :
3
Database :
MEDLINE
Journal :
American journal of medical genetics
Publication Type :
Academic Journal
Accession number :
8862628
Full Text :
https://doi.org/10.1002/(SICI)1096-8628(19960823)64:3<493::AID-AJMG9>3.0.CO;2-Q