Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis

Xiaoqian Ye, Audrey Guilmatre, Boris Reva, Inga Peter, Yann Heuzé, Joan T. Richtsmeier, Deborah J. Fox, Rhinda J. Goedken, Ethylin Wang Jabs, Paul A. Romitti

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background: 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. Methods: To screen for candidate genes for sagittal nonsyndromic craniosynostosis, the authors sequenced DNA of 93 sagittal nonsyndromic craniosynostosis patients from a population-based study conducted in Iowa and New York states. FGFR1-3 mutational hotspots and the entire TWIST1, RAB23, and BMP2 coding regions were screened because of their known roles in human nonsyndromic or syndromic sagittal craniosynostosis, expression patterns, and/or animal model studies. Results: The authors identified two rare variants in their cohort. A FGFR1 insertion c.730-731insG, which led to a premature stop codon, was predicted to abolish the entire immunoglobulin-like III domain, including the ligand-binding region. A c.439C>G variant was observed in TWIST1 at its highly conserved loop domain in another patient. The patient's mother harbored the same variant and was reported with jaw abnormalities. These two variants were not detected in 116 alleles from unaffected controls or seen in the several databases; however, TWIST1 variant was found in a low frequency of 0.000831 percent in Exome Aggregation Consortium database. Conclusions: The low mutation detection rate indicates that these genes account for only a small proportion of sagittal nonsyndromic craniosynostosis patients. The authors' results add to the perception that sagittal nonsyndromic craniosynostosis is a complex developmental defect with considerable genetic heterogeneity.

Original languageEnglish (US)
Pages (from-to)952-961
Number of pages10
JournalPlastic and reconstructive surgery
Volume137
Issue number3
DOIs
StatePublished - Mar 1 2016

All Science Journal Classification (ASJC) codes

  • Surgery

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