Genetics of Sensory Processing Dysfunction
Summary
Study Director: Elliott Sherr MD-PhD, and Elysa Marco MD
Sponsor: Wallace Research Foundation, the James Gates Family Foundation, the Brody Mickelson Family Foundation, the Gretsch Family, and the SNAP Crowdfunding community
Recruiting?: No
Official study title: Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction
Conditions studied: Sensory Processing Dysfunction
Purpose: This study suggests that SPD results from genetically coded, brain based differences, with monogenic and polygenic contributions. It highlights the importance of a thorough genetic evaluation in children presenting with sensory processing dysfunctions, regardless of the additional neurodevelopmental concerns.