Hypomandibular faciocranial dysostosis: another case and review

Am J Med Genet. 1993 Sep 1;47(3):352-6. doi: 10.1002/ajmg.1320470311.

Abstract

We report on a third case of hypomandibular faciocranial dysostosis and review the literature. Manifestations include craniosynostosis, prominent eyes, deficient midface and zygomatic arches, short nose with anteverted nares, protruding lower face, minute oral aperture, persistent buccopharyngeal membrane, and severe mandibular hypoplasia. In contrast to coronal synostosis found in the 2 earlier cases, our patient had multiple sutural synostosis. The 2 affected sibs reported earlier suggest the possibility of autosomal recessive inheritance. However, gonadal mosaicism for a dominant mutation or an undetected microdeletion must also be considered at this early stage in the delineation of this disorder.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Abnormalities, Multiple / pathology*
  • Craniofacial Dysostosis / genetics
  • Craniofacial Dysostosis / pathology*
  • Female
  • Genes, Recessive
  • Humans
  • Infant, Newborn
  • Mandible / abnormalities*