Article
Craniosynostosis.
European journal of human genetics : EJHG - 1 Apr 2011
Johnson David, Wilkie Andrew O M
Abstract excerpt
Craniosynostosis, defined as the premature fusion of the cranial sutures, presents many challenges in classification and treatment. At least 20% of cases are caused by specific single gene mutations or chromosome abnormalities. This article maps out approaches to clinical assessment of a child presenting with an unusual head shape, and illustrates how genetic analysis can contribute to diagnosis and management.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.