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Finding useful health information on the Internet can be difficult, but we’re here to help. This page gathers quality information from trusted sources. You can learn more about the disease, visit handpicked websites, and find resources to help you in your daily life. Need more information? Click the menu on the left to find more!

 

Wiskott Aldrich syndrome

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Overview

Type of Disease: Genetic, X-linked Congenital onset

Trusted Medical Sites

Genetic & Rare Diseases Information Center (GARD) GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

Support Organizations

Support organizations can provide help and guidance in areas such as peer matching, education and training, and therapy and counseling.

Disease Resources

Resources can help guide your quest for factual and reliable information.
Displaying 1-5 of 5 results.
Research Opportunities
Added On: Oct 26, 2012
Category: General
The foundation research program is used to motivate: 1. Novel and innovative research that will result in safer and less toxic cure 2. Studies to improve quality of life for patients 3. Studies to help understand WAS
About WAS
Added On: Oct 4, 2012
Category: General
This information and resource website, created in collaboration with physicians, researchers and patients. It serves as the primary source of information and online support for WAS families.
WAS Family and Patient Guide
Added On: Oct 4, 2012
Category: General
This guide answers the common questions asked by families of children with WAS. Included are the latest advances in medical care, clinical trials, and resources for families
WAS Family and Patient Guide
Added On: Oct 4, 2012
Category: General
This guide answers the common questions asked by families of children with WAS. Included are the latest advances in medical care, clinical trials, and resources for families.
Guide for Families and Patients
Added On: Oct 4, 2012
Category: General
This guide answers the common questions asked by families of children with WAS. Included are the latest advances in medical care, clinical trials, and resources for families.