Phelan-Mcdermid Syndrome – Bravelets

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Phelan-Mcdermid Syndrome

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About this cause:

Phelan-McDermid Syndrome, sometimes called 22q13 Deletion Syndrome, is a genetic condition caused by the deletion of the terminal end of chromosome 22 or mutation of the SHANK3 gene. In most cases, the condition is not inherited, but results from a de novo (spontaneous) mutation. Proceeds from Bravelets will benefit The Phelan-McDermid Syndrome Foundation.