Literature DB >> 8482284

Campomelic dysplasia--an underdiagnosed condition?

E K Normann1, J C Pedersen, G Stiris, C B van der Hagen.   

Abstract

Campomelic dysplasia (CD) is a rare skeletal dysplasia. The incidence, reported in the literature, is 0.05-0.09 per 10,000 live births. During the period December 1985-December 1990 there were 18,350 live births with 4 cases of CD at Aker University Hospital in Oslo, Norway. This gives an incidence of CD in our observation period of 2.2 per 10,000. Eliminating our first case, because of Pakistani decent, the total incidence is 1.6 per 10,000 among Norwegian infants which is much higher than the incidence previously mentioned. Perhaps CD is under-reported and a high proportion of patients remain undiagnosed. We present four cases and discuss the incidence.

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Year:  1993        PMID: 8482284     DOI: 10.1007/bf01956747

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  9 in total

1.  Birth prevalence rates of skeletal dysplasias.

Authors:  C Stoll; B Dott; M P Roth; Y Alembik
Journal:  Clin Genet       Date:  1989-02       Impact factor: 4.438

2.  The "campomelic" syndrome. Short life-span dwarfism with respiratory distress, hypotonia, peculiar facies, and multiple skeletal and cartilaginous deformities.

Authors:  F A Lee; H Isaacs; J Strauss
Journal:  Am J Dis Child       Date:  1972-10

3.  [The campomelic syndrome].

Authors:  P Maroteaux; J Spranger; J M Opitz; J Kucera; R B Lowry; R N Schimke; S M Kagan
Journal:  Presse Med       Date:  1971-05-22       Impact factor: 1.228

4.  Sex-reversed XY females with campomelic dysplasia are H-Y negative.

Authors:  F D Bricarelli; M Fraccaro; J Lindsten; U Müller; P Baggio; L D Carbone; A Hjerpe; F Lindgren; A Mayerová; H Ringertz; E M Ritzén; D C Rovetta; C Sicchero; U Wolf
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Campomelic dysplasia with sex reversal: morphological and cytogenetic studies of a case.

Authors:  C T Cooke; M T Mulcahy; G J Cullity; M Watson; P Srague
Journal:  Pathology       Date:  1985-07       Impact factor: 5.306

6.  Prenatal diagnosis of campomelic dwarfism.

Authors:  J P Fryns; K van den Berghe; A van Assche; H van den Berghe
Journal:  Clin Genet       Date:  1981-03       Impact factor: 4.438

7.  The birth prevalence rates for the skeletal dysplasias.

Authors:  I M Orioli; E E Castilla; J G Barbosa-Neto
Journal:  J Med Genet       Date:  1986-08       Impact factor: 6.318

8.  Campomelic dysplasia. Further elucidation of a distinct entity.

Authors:  B D Hall; J W Spranger
Journal:  Am J Dis Child       Date:  1980-03

Review 9.  The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

Authors:  C S Houston; J M Opitz; J W Spranger; R I Macpherson; M H Reed; E F Gilbert; J Herrmann; A Schinzel
Journal:  Am J Med Genet       Date:  1983-05
  9 in total
  4 in total

1.  Mild Campomelic Dysplasia: Report on a Case and Review.

Authors:  S Corbani; E Chouery; B Eid; N Jalkh; J Abou Ghoch; A Mégarbané
Journal:  Mol Syndromol       Date:  2011-01-10

2.  Congenital cervical instability in a patient with camptomelic dysplasia.

Authors:  Gregory P Lekovic; Harold L Rekate; Curtis A Dickman; Margaret Pearson
Journal:  Childs Nerv Syst       Date:  2006-03-23       Impact factor: 1.475

3.  A clinical and genetic study of campomelic dysplasia.

Authors:  S Mansour; C M Hall; M E Pembrey; I D Young
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

4.  Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.

Authors:  C Kwok; P A Weller; S Guioli; J W Foster; S Mansour; O Zuffardi; H H Punnett; M A Dominguez-Steglich; J D Brook; I D Young
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

  4 in total

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