Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 

Klippel Trenaunay Weber syndrome

Klippel Trenaunay Weber syndrome: Introduction

Klippel Trenaunay Weber syndrome: A rare genetic disorder characterized by benign skin growths made up of blood vessels, overgrowth of various limb tissues and varicose veins. More detailed information about the symptoms, causes, and treatments of Klippel Trenaunay Weber syndrome is available below.

Symptoms of Klippel Trenaunay Weber syndrome

Home Diagnostic Testing

Home medical testing related to Klippel Trenaunay Weber syndrome:

Wrongly Diagnosed with Klippel Trenaunay Weber syndrome?

Klippel Trenaunay Weber syndrome: Related Patient Stories

Klippel Trenaunay Weber syndrome: Complications

Review possible medical complications related to Klippel Trenaunay Weber syndrome:

Causes of Klippel Trenaunay Weber syndrome

Read more about causes of Klippel Trenaunay Weber syndrome.

Disease Topics Related To Klippel Trenaunay Weber syndrome

Research the causes of these diseases that are similar to, or related to, Klippel Trenaunay Weber syndrome:

Less Common Symptoms of Klippel Trenaunay Weber syndrome

Misdiagnosis and Klippel Trenaunay Weber syndrome

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem...read more »

Klippel Trenaunay Weber syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Klippel Trenaunay Weber syndrome: Animations

Statistics for Klippel Trenaunay Weber syndrome

Klippel Trenaunay Weber syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Klippel Trenaunay Weber syndrome, or answer someone else's question, on our message boards:

Definitions of Klippel Trenaunay Weber syndrome:

Klippel Trenaunay Weber syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Klippel Trenaunay Weber syndrome, or a subtype of Klippel Trenaunay Weber syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Klippel Trenaunay Weber syndrome as a "rare disease".
Source - Orphanet

 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise