# 22q13.3 deletion syndrome | Developmental Synaptopathies Consortium

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An NIH-Funded Rare Diseases Clinical Research Network Consortium

Another name for Phelan McDermid Syndrome. PMS occurs due to a loss of a region labeled q13.3 on chromosome 22.

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The Developmental Synaptopathies Consortium (DSC) is part of the Rare Diseases Clinical Research Network (RDCRN), which is funded by the National Institutes of Health (NIH) and led by the National Center for Advancing Translational Sciences (NCATS) through its Division of Rare Diseases Research Innovation (DRDRI). DSC is funded under grant number U54NS092090 as a collaboration between NCATS, the National Institute of Neurological Disorders and Stroke (NINDS), the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), and the National Institute on Deafness and Other Communication Disorders (NIDCD). This website is hosted by the network’s Data Management and Coordinating Center at Cincinnati Children’s Hospital Medical Center, which is funded by NCATS and NINDS under grant number TR002818. The content of this website is solely the responsibility of the DSC administrative coordinating center at Boston Children’s Hospital and does not necessarily represent the official views of the NIH.

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