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Supporting Families. Advancing Research.

Weiss-Kruszka Research Foundation connects families, clinicians, and researchers to enhance the understanding of Weiss-Kruszka Syndrome, fostering support and awareness for those affected by this rare genetic condition.

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Newly diagnosed?

You don’t have to navigate this alone. We’re here to help you understand this diagnosis with clarity and support.

WKS Patient Registry

A secure, voluntary registry that collects clinical, genetic, and demographic data to advance research and improve care.

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