Klippel-Trenaunay-Weber Syndrome

Overview

A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Klippel-Trenaunay-Weber Syndrome

Topic type

Condition

Category

Cardiology

MeSH classification

C14.907.077.410

Preparing for an appointment about Klippel-Trenaunay-Weber Syndrome

If you are speaking with a healthcare professional about Klippel-Trenaunay-Weber Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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