Literature DB >> 18326400

[Genetics of craniofacial development].

L N A van Adrichem1, A J M Hoogeboom, E B Wolvius.   

Abstract

Congenital craniofacial malformations vary widely in both expression and gravity. To understand congenital craniofacial malformations, knowledge of embryonic development is of essential importance. Craniosynostosis has its origin in the failure of suture development between 2 bone centres or in early closure of the suture by bone centre tissue fusion. Hereditary craniosynostosis phenotypes predominantly arise by autosomal dominant inheritance. So far, the majority of mutations have been found in fibroblast growth-factor receptor genes (FGFR-genes). Different phenotypes are not primarily created by disparities of the receptors, but particularly by tissue-specific expressions.

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Year:  2008        PMID: 18326400

Source DB:  PubMed          Journal:  Ned Tijdschr Tandheelkd        ISSN: 0028-2200


  1 in total

Review 1.  Craniosynostosis - Recognition, clinical characteristics, and treatment.

Authors:  Nina Kajdic; Peter Spazzapan; Tomaz Velnar
Journal:  Bosn J Basic Med Sci       Date:  2018-05-20       Impact factor: 3.363

  1 in total

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