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![1 in 25,000](https://smsresearchfoundation.org/wp-content/uploads/2020/04/45828061_1959431707467844_1625876478539333632_n.jpg)
1 in 25,000
…live births in the US are affected by SMS. Identified only in 1982, the SMS Research Foundation is working tirelessly to fund research to improve the treatment options and lives of SMS children.
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What is SMS?
Smith-Magenis Syndrome is a complex developmental disorder that affects multiple organ systems of the body. The disorder is characterized by a pattern of abnormalities that are present at birth (congenital) as well as behavioral and cognitive problems.
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Our Mission
It is our goal to advance the scientific understanding of this rare syndrome so that effective treatments can be developed to improve the cognitive delays and behavioral issues of those living with SMS.
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Who We Are
The SMS Research Foundation supports research to improve the knowledge and understanding of Smith-Magenis Syndrome.
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Get Involved
It’s your support that keeps our life-changing research programs going, and brings hope to families facing this challenge.
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