rss
J Med Genet 1993;30:683-686 doi:10.1136/jmg.30.8.683
  • Research Article

Campomelic dysplasia: evidence of autosomal dominant inheritance.

  1. S A Lynch,
  2. M L Gaunt,
  3. A M Minford
  1. Department of Genetics, Leeds General Infirmary, UK.

      Abstract

      We present a mother and daughter with clinical and radiological findings consistent with the diagnosis of campomelic dysplasia. Milder tibial bowing and significant shortening of the phalangeal bones of both hands and feet may distinguish this from the classical autosomal recessive form of the disease.

      Register for free content

      The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

      Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.