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About us
WHO WE ARE
We are a global Foundation with branches in the United States, Europe and Australia. Together we advocate and fund work aimed at enhancing the lives of patients affected by WWOX-related diseases.
OUR MISSION
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To provide a support framework for families with children suffering from WWOX deficiency.
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Fund researchers to pursue scientific research related to WWOX.
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Connect WWOX patients with WWOX researchers and Industry Partners for ongoing clinical studies through our Patient Registry.
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Assist researchers to better understand the phenotypic spectrum of WWOX patients.
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Raise awareness to the general public and the medical community to allow quick and accurate diagnosis of WWOX related syndromes.
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