
Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis
Author(s) -
Xiaoqian Ye,
Audrey Guilmatre,
Boris Reva,
Inga Peter,
Yann Heuzé,
Joan T. Richtsmeier,
Deborah Fox,
Rhinda Goedken,
Ethylin Wang Jabs,
Paul A. Romitti
Publication year - 2016
Publication title -
plastic and reconstructive surgery/psef cd journals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.841
H-Index - 179
eISSN - 1076-5751
pISSN - 0032-1052
DOI - 10.1097/01.prs.0000479978.75545.ee
Subject(s) - craniosynostosis , medicine , genetics , biology
Craniosynostosis is a condition that includes the premature fusion of one or multiple cranial sutures. Among various craniosynostosis forms, sagittal nonsyndromic craniosynostosis is the most prevalent. Although different gene mutations have been identified in some craniosynostosis syndromes, the cause of sagittal nonsyndromic craniosynostosis remains largely unknown.