Literature DB >> 15558723

A novel syndrome resembling Desbuquois dysplasia.

Ali Al Kaissi1, N Nessib, M B Ghachem, A Hammou, N Guiddana, K Kozlowski.   

Abstract

We report on three Tunisian siblings with a rare assortment of clinical and radiographic abnormalities closely resembling Desbuquois dysplasia. However, the siblings have had normal facies, normal hands, and were mentally normal. There were severe musculo-skeletal distinguishing features such as joint stiffness, severe kyphoscoliosis, and multiple large joint dislocations. Moreover, the patients had an additional remarkable radiographic feature not reported in Desbequois dysplasia-multiple carpal ossification centers. The diagnosis of Desbuquois dysplasia is more difficult in older children and adults as the characteristic facial features of early childhood may recede, and the metaphyseal growth plates obliterate. This condition of these patients represents a novel Desbuquois-like syndrome. (c) 2004 Wiley-Liss, Inc.

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Year:  2005        PMID: 15558723     DOI: 10.1002/ajmg.a.30344

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Radiographic findings of Desbuquois dysplasia.

Authors:  Meltem Özdemir; Rasime Pelin Kavak
Journal:  BJR Case Rep       Date:  2020-11-02

2.  Synophyrs, curly eyelashes and Ptyrigium colli in a girl with Desbuquois dysplasia: a case report and review of the literature.

Authors:  Ali Al Kaissi; Klaus Klaushofer; Franz Grill
Journal:  Cases J       Date:  2009-09-15

3.  Advanced ossification of the carpal bones, and monkey wrench appearance of the femora, features suggestive of a propable mild form of desbeqious dysplasia: a case report and review of the literature.

Authors:  Ali Al Kaissi; Christof Radler; Klaus Klaushofer; Franz Grill
Journal:  Cases J       Date:  2009-01-13
  3 in total

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