Bringing everyone to the table – findings from the 2018 Phelan-McDermid Syndrome Foundation International Conference | Orphanet Journal of Rare Diseases | Full Text

Bringing everyone to the table – findings from the 2018 Phelan-McDermid Syndrome Foundation International Conference | Orphanet Journal of Rare Diseases | Full Text

Bringing everyone to the table – findings from the 2018 Phelan-McDermid Syndrome Foundation International Conference

Phelan-McDermid Syndrome (PMS) is a rare neurodevelopmental disorder characterized by global developmental delay, autism spectrum disorder, and numerous systemic complications including seizures, gastrointesti...

Authors:Kimberly Goodspeed, Geraldine Bliss and Diane Linnehan

Citation:Orphanet Journal of Rare Diseases 2020 15:152

Content type:Research

 

Published on: 16 June 2020

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