NDIS Support for Phelan-McDermid Syndrome in Byron Bay, NSW

Phelan-McDermid Syndrome (PMS), also known as 22q13.3 deletion syndrome, is a rare genetic condition caused by deletion or disruption of the terminal region of chromosome 22, commonly involving the SHANK3 gene. SHANK3 plays a critical role in synapse formation in the brain, and its loss is one of…