Smith-Magenis syndrome is a complex condition 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 issues.

Common symptoms include distinctive facial features, skeletal malformations, varying degrees of intellectual disability, speech and motor delays, sleep disturbances, and self-injurious or attention-seeking behaviors. 

Resources

National Organization for Rare Disorders is a non-profit patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. 

Smith-Magenis Research Foundation aims to advance scientific research leading to innovative treatment options for people living with Smith-Magenis Syndrome.