Overview
Williams-Beuren Syndrome (WBS) is a rare genetic disorder caused by the deletion of a collection of genes on chromosome 7. It is characterized by a distinct facial appearance, developmental and cognitive delays, and an increased risk of cardiovascular problems. Affected individuals often have a friendly personality, an affinity for music, and an affinity for water. WBS is associated with a wide range of medical issues and can have lifelong effects on those affected. Treatment involves managing the varying symptoms associated with WBS, which may include physical and occupational therapies, speech therapy, and educational and behavioral interventions. Early diagnosis is an important part of treatment and management of the condition. With proper care, individuals with WBS can lead a fulfilling and productive life.