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Tourette Syndrome
Child Development >Tourette Syndrome > CDC-funded Research and Projects

CDC-funded Research and Projects

National Tourette Syndrome Association (TSA)
Tourette Syndrome Education and Outreach to Service Providers: CDC’s National Center on Birth Defects and Developmental Disabilities has a cooperative agreement with the Tourette Syndrome Association to support provider education and intensive training for healthcare professionals, educators, allied caregivers, and the general public.

Pennsylvania Tourette Syndrome Association
Tourette Syndrome Public Health Improvement Project: This program supports educational and informational services targeted to Pennsylvania citizens who have Tourette Syndrome, their families, and the surrounding community. Pennsylvania is a state chapter of the National Tourette Syndrome Association.

University of Oklahoma Health Sciences Center
To better understand the prevalence of TS and its public health impact, the University of Oklahoma Health Sciences Center, in collaboration with the NCBDDD scientists, has initiated a pilot epidemiology study of Tourette Syndrome and tics in school-age children.

University of Washington
Descriptive Study of Tourette Syndrome Quality of Life: This research study will identify factors that contribute to the quality of life of persons with Tourette Syndrome. This work is a collaborative effort with the Association of University Centers on Disabilities (AUCD), the University of Washington, and the National Center on Birth Defects and Developmental Disabilities.

Date Last Reviewed: May 27, 2008
Page last updated: May 27, 2008
Content source: National Center on Birth Defects and Developmental Disabilities

 

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National Center on Birth Defects and Developmental Disabilities

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