Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients

Clin Genet. 1989 Feb;35(2):157-60. doi: 10.1111/j.1399-0004.1989.tb02922.x.

Abstract

In this report we present two unrelated patients with the postaxial dysostosis syndrome (Miller syndrome) and document further the phenotypic variability of the craniofacial stigmata and of the postaxial (and preaxial) upper and lower limb reduction anomalies.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child
  • Dysostoses / genetics*
  • Facial Bones / abnormalities*
  • Female
  • Fingers / abnormalities*
  • Humans
  • Infant
  • Male
  • Phenotype
  • Syndrome
  • Toes / abnormalities*