This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Aetiology

Authoring team

The aetiology of ulnar dysplasia is unknown but suggested theories include:

  • genetic:
    • sporadic gene mutation most frequent
    • occasionally autosomal dominant familial predisposition
    • syndromic associations, inherited in an autosomal dominant manner:
      • orofacial malformations
      • Cornelia de Lange's syndrome
      • Schinzel Syndrome
      • femur-fibula-ulna syndrome
  • extrinsic:
    • hormonal exposure
    • no clear link with thalidomide exposure

One pathogenetic theory is that of an injury to the zone of polarizing activity which dictates the morphogen gradient governing antero-posterior patterning

 


Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.