Literature DB >> 8862628

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

J S Fryburg1, T E Kelly.   

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.

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Year:  1996        PMID: 8862628     DOI: 10.1002/(SICI)1096-8628(19960823)64:3<493::AID-AJMG9>3.0.CO;2-Q

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from India.

Authors:  S R Phadke; N Gupta; K M Girisha; M Kabra; M Maeda; E Vidal; A Moser; S Steinberg; R D Puri; I C Verma; N Braverman
Journal:  J Appl Genet       Date:  2010       Impact factor: 3.240

  1 in total

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