Mandibular dysostosis without microphthalmia caused by OTX2 deletion

Am J Med Genet A. 2016 Sep;170(9):2466-70. doi: 10.1002/ajmg.a.37837. Epub 2016 Jul 5.

Abstract

Mutations in OTX2 are mostly identified in patients with anophthalmia/microphthalmia with variable severity. The OTX2 homeobox gene plays a crucial role in craniofacial morphogenesis during early embryo development. We report for the first time a patient with a mandibular dysostosis caused by a 120 kb deletion including the entire coding sequence of OTX2, identified by array CGH. No ocular malformations were identified after extended ophthalmologic examination. Our data refine the clinical spectrum associated with OTX2 mutations and suggests that OTX2 haploinsufficiency should be considered as a possible cause for isolated mandibular dysostosis. © 2016 Wiley Periodicals, Inc.

Keywords: OTX2 haploinsufficiency; craniofacial development; dysgnathia; mandibular dysostosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosome Breakpoints
  • Chromosomes, Human, Pair 14
  • Comparative Genomic Hybridization
  • Facies
  • Female
  • Gene Deletion*
  • Genetic Association Studies*
  • Heterozygote
  • Humans
  • Mandibulofacial Dysostosis / diagnosis*
  • Mandibulofacial Dysostosis / genetics*
  • Microphthalmos
  • Otx Transcription Factors / genetics*
  • Phenotype*
  • Sequence Deletion

Substances

  • Otx Transcription Factors