Literature DB >> 2002481

Pitfalls in counselling: the craniosynostoses.

R Marini1, K Temple, L Chitty, S Genet, M Baraitser.   

Abstract

We describe three families to highlight the variability of expression and penetrance that can occur in the craniosynostoses. In two of the families, gene carriers were only identified in retrospect by looking at photographs of other family members. In the third family, identical twins were initially thought to be discordant for sagittal craniosynostosis until early skull x rays were examined and both were found to be affected. The dilemmas faced when counselling these families are discussed.

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Year:  1991        PMID: 2002481      PMCID: PMC1016780          DOI: 10.1136/jmg.28.2.117

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  Crouzon Syndrome. A clinical and roentgencephalometric study.

Authors:  S Kreiborg
Journal:  Scand J Plast Reconstr Surg Suppl       Date:  1981

2.  Germinal mosaicism in Crouzon syndrome.

Authors:  B R Rollnick
Journal:  Clin Genet       Date:  1988-03       Impact factor: 4.438

3.  An autosomal recessive form of craniofacial dysostosis (the Crouzon syndrome).

Authors:  R C Juberg; S R Chambers
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

4.  A family study of craniosynostosis, with probable recognition of a distinct syndrome.

Authors:  C O Carter; K Till; V Fraser; R Coffey
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318

  4 in total

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