Literature DB >> 12949976

Cervical spine stenosis and possible vitamin K deficiency embryopathy in an unusual case of chondrodysplasia punctata and an updated classification system.

Delaina D Eash1, David D Weaver, Nicola Brunetti-Pierri.   

Abstract

We describe in this paper a patient with brachytelephalangic chondrodysplasia punctata (BCDP) who has multiple serious medical problems and striking physical abnormalities. These include cervical spine stenosis with resultant quadriplegia, severe nasal hypoplasia, and brachytelephalangy. Radiographs taken shortly after birth demonstrated extensive epiphyseal and vertebral stippling, and distal phalangeal hypoplasia. The pregnancy was complicated by maternal intestinal obstruction due to a small bowel carcinoma and probable malabsorption. The severity of the phenotype in this case may have been influenced by these maternal factors particularly vitamin K deficiency. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12949976     DOI: 10.1002/ajmg.a.20242

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


  5 in total

Review 1.  Natural history and management of cervical spine disease in chondrodysplasia punctata and coumarin embryopathy.

Authors:  Timothy W Vogel; Arnold H Menezes
Journal:  Childs Nerv Syst       Date:  2012-01-25       Impact factor: 1.475

2.  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

Review 3.  Maternal mixed connective tissue disease and offspring with chondrodysplasia punctata.

Authors:  Steffan W Schulz; Michael Bober; Caitlyn Johnson; Nancy Braverman; Sergio A Jimenez
Journal:  Semin Arthritis Rheum       Date:  2008-12-24       Impact factor: 5.532

4.  Clinical and radiological pictures of two newborn babies with manifestations of chondrodysplasia punctata and review of available literature.

Authors:  Elżbieta Jurkiewicz; Beata Marcinska; Joanna Bothur-Nowacka; Anna Dobrzanska
Journal:  Pol J Radiol       Date:  2013-04

5.  Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss.

Authors:  Irena Vrečar; Gorazd Rudolf; Borut Peterlin; Luca Lovrecic
Journal:  Mol Cytogenet       Date:  2015-10-31       Impact factor: 2.009

  5 in total

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