This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Prader-Willi syndrome

Authoring team

Prader-Willi syndrome is a disorder which affects 1 in 15000 births and is characterised by:

  • neonatal hypotonia
  • behavioural disturbance, particularly hyperphagia
  • mild-to-moderate mental retardation

60% of cases have a small deletion of the paternal chromosome 15q11-13. The majority of the remainder have two apparently normal apparently normal (but maternally inherited) chromosome 15s (See genetics section for more details).


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.