Smith-Lemli-Opitz Foundation
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Mission Statement
The Smith-Lemli-Opitz Foundation works worldwide to improve the quality of life for people with Smith-Lemli-Opitz syndrome through education, family support, awareness, and funding research into the disorder.
About This Cause
Smith-Lemli-Opitz syndrome (SLOS) is a rare genetic condition caused by an inborn error in cholesterol synthesis. Since cholesterol is an essential component of the cell membrane and tissues of the brain, decreased levels can lead to growth and developmental delays, as well as distinct physical abnormalities. Founded in 1990, the Smith-Lemli-Opitz Foundation works to provide parents with an informational website & parental support group, access to SLOS specialists, and national family & medical conferences. The Foundation also works to fund grants into SLOS-related research. All services and programs are 100% free to families. The Foundation is run by volunteer parents and a dedicated board of directors and staff. Their medical advisory board includes specialists who work tirelessly to find a cure for SLOS.