| Literature DB >> 18391497 |
Abstract
Disruption of normal suture development and function can result in premature suture fusion, craniosynostosis. This review focuses on syndromic forms of craniosynostosis. More than 100 syndromes in which craniosynostosis is a feature have been documented and here the most common conditions including Apert and Crouzon syndromes are described as well as other conditions with a particularly interesting molecular etiology, such as Saethre- Chotzen and craniofrontonasal syndrome.Entities:
Mesh:
Year: 2008 PMID: 18391497 DOI: 10.1159/000115034
Source DB: PubMed Journal: Front Oral Biol ISSN: 0301-536X