William Syndrome

Neurophilosophy

Tag archives for William Syndrome

WILLIAMS Syndrome (WS) is a rare neurodevelopmental disorder caused by the deletion of about 28 genes from the long arm of chromosome 7. It is characterized by mild to moderate mental retardation and “elfin” facial features. Most strikingly, individuals with WS exhibit highly gregarious social behaviour: they approach strangers readily and indiscriminately, behaving as if…