This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages without signing in

Milroy's syndrome

Authoring team

Milroy's disease is a congenital familial primary lymphoedema which results from vertical autosomal inheritance of a single gene. Typically, it presents as asymmetric swelling of the legs.

It is a rare disease accounting for about 2% of primary lymphoedemas. Men and women are equally affected.


Related pages

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.