Werner Syndrome

A Genetic Disease that Mimics Premature Aging

Department of

Werner Syndrome Patient
Useful Information About
Werner Syndrome
and the WRN Gene:

Werner Syndrome International Registry

This site contains diagnostic criteria for WRN
and contact information for a central repository
of WS data and research and materials.

WRN  Mutational Database

A compilation of WS associated WRN mutations.

Werner Syndrome (WS) is an uncommon, autosomal recessive human genetic disease that mimics premature aging. Patients with WS appear to age rapidly following puberty, and are at increased risk of developing cancer and cardiovascular disease. Symptoms of WS include premature graying and loss of hair, bilateral cataracts, osteoporosis, atherosclerosis, diabetes and scleroderma-like changes and ulceration of the skin.

The WS associated gene has been identified and named WRN.

This website was primarily designed as a resource for clinicians and basic scientists interested in WS medicine and biology.

Please read the disclaimer.

WS International Registry     |     WRN Mutational Database

Department of Pathology     |     School of Medicine     |     University of Washington

Last updated: Jan. 04, 2019
by: Jiaming Zhang

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Department of Pathology
University of Washington
Seattle, Washington 98105 USA
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