Literature DB >> 1481849

Chondrodysplasia punctata: another possible X-linked recessive case.

C P Bennett1, A C Berry, D J Maxwell, M J Seller.   

Abstract

A 22-week fetus who had died in utero had a markedly hypoplastic nose and other facial abnormalities, short fingers, hypoplastic nails, and small phallus. Radiologically there was symmetrical cartilaginous stippling of the vertebral column, femoral heads, calcanei and elbows typical of chondrodysplasia punctata (CP), and metacarpal shortness and tiny pyramidal phalanges. The several causally different forms of CP are tabulated. Differential diagnosis suggests that the present case, which does not have limb shortness, could be a case of X-linked recessive brachytelephalangic chondrodysplasia punctata.

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Year:  1992        PMID: 1481849     DOI: 10.1002/ajmg.1320440615

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


  3 in total

1.  Brachytelephalangic chondrodysplasia punctata with severe spinal cord compression: report of four new cases.

Authors:  Arnaud Garnier; Stéphane Dauger; Danièle Eurin; Ida Parisi; Giancarlo Parenti; Catherine Garel; Katy Delbecque; Clarisse Baumann
Journal:  Eur J Pediatr       Date:  2006-08-26       Impact factor: 3.183

2.  Maternal systemic lupus erythematosus and chondrodysplasia punctata in two sibs: phenocopy or coincidence?

Authors:  N Elçioglu; C M Hall
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

3.  Brachytelephalangic chondrodysplasia punctata: A difficult diagnosis.

Authors:  Andrea Sanfilippo; Stefano Bartoletti
Journal:  Radiol Case Rep       Date:  2015-11-06
  3 in total

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