Williams Syndrome
Williams Syndrome (WS) is a rare genetic disorder caused by the deletion of multiple genes located on chromosome 7. It is characterized by a combination of medical, physical and cognitive problems. People with Williams Syndrome often have a distinctive facial appearance, mild intellectual disability, cardiovascular and mouth/dental anomalies, and musculoskeletal and auditory abnormalities. The social behavior of people with WS is also distinctive, characterized by an engaging personality, strong social skills and interest, and extreme interest in music. Diagnosis is usually made through genetic testing, and treatment focuses on managing the associated health problems and providing support for the individual and family. Williams Syndrome serves as an important model for understanding the impact of genetic changes on human development.
← Journal of Hereditary Diseases