Article
Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis.
Genetics in medicine : official journal of the American College of Medical Genetics - 1 Apr 2014
Greenwood Jaclyn, Flodman Pamela, Osann Kathryn, Boyadjiev Simeon A, Kimonis Virginia
Abstract excerpt
PURPOSE: Craniosynostosis is a common cranial malformation occurring in 1 per 2,000-2,500 births. Isolated defects (nonsyndromic) occur in ~75% of cases and are thought to have multifactorial etiology. It is believed that each suture synostosis is a distinct disease, with varying phenotypes and recurrence rates. METHODS: We analyzed family histories of 660 mutation-negative nonsyndromic craniosynostosis patients...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
