Auriculo-condylar syndrome: additional patients

Am J Med Genet. 2002 Oct 1;112(2):209-14. doi: 10.1002/ajmg.10631.

Abstract

This report describes several relatives in three generations of one family and another, unrelated boy with auriculo-condylar syndrome, a rare autosomal dominant disorder. Variation in the severity of the abnormalities was observed. We discuss the findings in our patients in relation to those in the literature.

Publication types

  • Case Reports

MeSH terms

  • Branchial Region / abnormalities
  • Child
  • Ear / abnormalities*
  • Female
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Mandible / abnormalities
  • Pedigree