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Donate Now
  • Home
  • About SMS
    • What Is SMS?
    • Living with SMS
      • SMS Clinics
      • A Community That Cares
      • Early Intervention
      • Behavior
      • Speech & Language
      • Sleep
      • Medical Management & Treatment
      • Medication
      • Guardianship & Financial Planning
    • FAQ
  • Education
    • SMS Conference
      • Conference FAQ
      • Support the Conference
      • Conference Sponsor/Exhibitor
      • Keynote Speaker
      • Thursday Workshops
      • #SMSPossibilities Campaign
      • Conference Costs
      • Conference Information
    • Webinars
    • For the Parent/Caregiver
    • For the Health Professional
    • For the Educator
    • For the Sibling
    • For the Individual with SMS
    • Publications & Resources
  • Awareness
    • Awareness Toolbox
    • PRISMS Store
    • SMS Awareness Day
    • PRISMS Blog
      • Share Your Story
    • International Partners
      • Together for Hope – Collaboration
    • Rare Disease Day
  • Research
    • Research at PRISMS
    • 2019 SMS Research Symposium
    • SMS Patient Registry
    • Active Research
      • Postdoctoral Fellowship
      • Brain Donor Project
    • Research Publications
  • Get Involved
    • Donate
    • Join our Community
    • Fundraising
    • 17p11.2 Society
    • Volunteering
    • Regional Representatives
  • Who We Are
    • The Mission
    • The Team
    • The Work
    • The History
    • Contact Us
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PRISMS, Parents and Researchers Interested In Smith-Magenis Syndrome, is dedicated to providing information and support to families of persons with Smith-Magenis Syndrome (SMS), sponsoring research and fostering partnerships with professionals to increase awareness and understanding of SMS.

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Many photos throughout the PRISMS website are courtesy of Rick Giudotti, Positive Exposure.

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