Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1988 Jul;25(7):491–493. doi: 10.1136/jmg.25.7.491

Auralcephalosyndactyly: a new hereditary craniosynostosis syndrome.

T W Kurczynski 1, S M Casperson 1
PMCID: PMC1050527  PMID: 2845086

Abstract

A family is described in which craniosynostosis is associated with characteristic pinnae, a short columella, and symmetrical syndactyly of the fourth and fifth toes, inherited as an autosomal dominant condition. Various dominantly inherited syndromes involving craniosynostosis have been identified, but the constellation of findings in this family suggests a new syndrome different from those previously described.

Full text

PDF
491

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. PFEIFFER R. A. DOMINANT ERBLICHE AKROCEPHALOSYNDAKTYLIE. Z Kinderheilkd. 1964 Sep 16;90:301–320. [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES