Information. Research. Action.
Fighting Wolfram Syndrome
Ashkenazi Variant
Ashkenazi Jewish WFS1-Associated Wolfram Syndrome
Wolfram syndrome is a rare genetic disorder that primarily affects the nervous system and other body systems. A specific subtype — Ashkenazi Jewish WFS1-Associated Wolfram Syndrome — impacts individuals of Ashkenazi Jewish descent.
Learn more about the unique features that distinguish the Ashkenazi variant.
Common Symptoms
Ashkenazi Jewish WFS1-Associated Wolfram syndrome can cause vision loss, atypical diabetes, urinary issues and neurological concerns. Learn more about potential symptoms now.
Ongoing Research and Resources
Washington University in St. Louis’ internationally recognized team is actively seeking new patients to join their clinical care and research efforts. Join the Wolfram Syndrome International Registry to learn about clinical studies and genetic testing opportunities.
How Does a Diagnosis Affect Family Planning?
Jewish Wolfram syndrome is a recessive condition — both parents must be carriers for a child to be affected. Learn more about genetic inheritance, family planning, carrier testing and reproductive options.
I think my diagnosis really made me appreciate my life and pushed me to experience as much as I could… It's a matter of thinking outside-the-box about what your limitations are, and what you can do with them.”
— Cathy G., age 69
Stay in Touch
Feel free to contact us with any questions.
Email
JewishWolframNetwork@gmail.com