Our Story
Families Leading the Way
WWOX Europe e.V. was founded by parents of a child affected by a WWOX-related disorder. The foundation serves as a point of contact for families across Europe and aims to strengthen connections, information sharing and mutual support within the WWOX community.
The aims of WWOX Europe e.V. are to:
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Promoting science, research and development related to WWOX syndromes in Europe.
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To promote, maintain and disseminate awareness and knowledge about WWOX syndromes.
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The support of and exchange between affected European families
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Representation of the interests of affected children vis-à-vis research institutions and public authorities.
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Cooperation with domestic and foreign associations sharing a common goal.
A Registered Charitable Association in Germany
Recognised by the Tax Authority Mainz - 21 February 2024
Tax No 26/675/17974 - Local Court of Mainz VR 42350
Board of Directors
Alexander Maringer
Chairman
Alexander and his wife Anne founded the association to establish a European representative office of the WWOX Foundation. He was elected chairman by the general assembly.
Alexander works as an in-house lawyer in the pharmaceutical industry and thus brings a lot of experience and knowledge regarding medical research, development and clinical trials to the .
Alexander is the father of Marius, who suffers from WOREE syndrome, and his big sister Regina. The family lives in Mainz, Germany.
Anne Maringer
Deputy Chairwoman
Anne founded the foundation together with her husband Alexander and acts as deputy chairwoman of WWOX Europe e.V.
Anne works in the IT consulting industry. In addition, she cares for her son Marius, who suffers from WOREE syndrome.
Help Move WWOX Research Forward
Your support helps fund research, strengthen family resources and build a brighter future.
One Foundation. A Global Mission
Working with partners at home and abroad to advance research, strengthen family support and build awareness.
