Resources- Specific Diagnosis Card Catalog- Smith-Magenis Syndrome

Who to Contact

PRISMS (Parents & Researchers Interested in Smith-Magenis Syndrome)
P.O. Box 741914
Dallas, TX 75374-1914
Phone: 972.231.0035
Fax: 413.826.6539
E-mail: info@prisms.org
Web: www.prisms.org

PRISMS is dedicated to providing information and support to families of persons with Smith-Magenis Syndrome (SMS) and fostering partnerships with professionals to increase awareness and understanding of SMS.

PRISMS serves as a central clearinghouse for information about SMS, providing a range of educational and support services, including telephone support; database of registered families; official newsletter - Spectrum; information packet, brochures for families, caregivers & medical professionals; Parent-to-Parent Program; and an International conferences on SMS

Where to Go Chat with Others

Smith-Magenis Syndrome Mailing List
The SMS Mailing list is designed to promote the exhange of information and communication about Smith-Magenis syndrome among parents, professionals and researchers working with this condition. Members of the SMS Mailing list will include parents and/or relatives of persons with SMS, as well as special educators, health professionals and researchers working specifically with this rare condition.

Learn More About It

What is Smith-Magenis Syndrome?
From the Prisms web site

What is SMS?

Smith-Magenis Syndrome
From the Online Mendelian Inheritance of Man (OMIM)

Smith-Magenis Syndrome: Genetic Research
From the Department of Neurology at Baylor College of Medicine

Smith-Magenis Syndrome: Report of Two Cases and Review of the Literature
From AbdelKarim A. Al-Qudah, MD(ABCN); Mohammed S. El-Khateeb, PhD; Walid Abu-Hamour, MD; Najwa Khoury Bulos, MD, FAAP

Links

PRISMS (Parents and Researchers Interested in Smith-Magenis Syndrome)

Smith-Magenis Syndrome Research
Baylor College of Medicine

Smith Magenis Syndrome Foundation
United Kingdom

Le Syndrome de Smith Magenis
France