This site is intended for healthcare professionals

Sign in
Go to /sign-in page

You can view 5 more pages without signing in

Genetics

Authoring team

Usher's syndrome is inherited in an autosomal recessive manner.

There are at least seven genes responsible for the various forms of the syndrome.

One of the more common genes is USH1B which is found on chromosome 11q13.5 (1). The gene codes for a defective myosin VIIA protein. Cytoskeletal abnormalities may be important in the pathogenesis of the other forms of Usher's syndrome.

Reference:

  • Weil, D. et al. (1995). Defective myosin VIIA gene responsible for Usher syndrome type 1A. Nature, 374, 60-1.

Related pages

Create an account to add page annotations

Create a free account

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.