This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Clinical features

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Sturge-Weber syndrome is characterised by:

  • a capillary naevus or port wine stain which is unilateral and usually over the forehead and eyelid conforming to the 1st or the 1st and 2nd divisions of the trigeminal nerve
  • epilepsy occurs in 90%, usually presenting in infancy
  • developmental delay - particularly of speech - and behavioural disorders occur in 50%
  • hemiparesis and homonymous hemianopia occur in 30%
  • there may be glaucoma in the affected eye

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.