You are here

  • Home
  • Archive
  • Volume 28, Issue 10
  • Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype.

Article Text

Article menu

PDF

Research Article
Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype.
  1. A L Ogilvy-Stuart,
  2. A C Parsons
  1. Department of Paediatrics, Taranaki Base Hospital, New Plymouth, New Zealand.

    Abstract

    A sibship with postaxial acrofacial dysostosis syndrome (Miller syndrome) is reported. In addition to the characteristic facial and limb defects, previously undescribed anomalies, including midgut malrotation, gastric volvulus, and renal anomalies, are recorded.

    http://dx.doi.org/10.1136/jmg.28.10.695

    Statistics from Altmetric.com

      Request Permissions

      If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.