This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

EEC syndrome

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) is an autosomal dominant condition with variable penetrance comprising:

  • ectrodactyly
  • ectodermal dysplasia
  • facial clefting including cleft lip and palate

Common associated features include:

  • vesicoureteric reflux leading to recurrent urinary tract infections
  • nasolacrimal duct obstruction leading to tearing
  • hypopigmentation
  • hypoplasia or absence of teeth

There are thought to be three different forms of EEC syndrome with phenotypic similarities but different gene abnormalities(1).

 

Ref: (1) van Bokhoven H et al. (2001). Am J Hum Genet 69: 481-492.


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.