Patient Organizations

Connecting with organizations and the larger rare disease community can provide valuable resources, information, and support for parents, families, and patients affected by a central nervous system (CNS) disease diagnosis.*

MPS/MPSIIIA

GM1 / GM2

* This is not intended as a comprehensive list of all global organizations. For assistance finding additional resources, please Contact us.

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Lysogene COVID-19 update

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Don’t hesitate to contact us if you need more help.