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MSL3 Syndrome Foundation
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Events

TWO Virtual Meet-Ups (February 27th-28th) in recognition of Rare Disease Day. Find the details in our Facebook Support group here:

https://www.facebook.com/groups/337289080167162/

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MSL3 Syndrome Foundation is spreading awareness about MSL3 Syndrome, offering support and resources to families navigating this challenging genetic disorder, and raising funds in support of research and treatment of MSL3 Syndrome.

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We want to hear from you. Email us at msl3foundation@gmail.com.

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