Williams Syndrome
Williams syndrome is a rare genetic condition (estimated to occur in 1/10,000 births) which causes medical and developmental problems.
Williams syndrome was first recognized as a distinct entity in 1961. It is present at birth, and affects males and females equally. It can occur in all ethnic groups and has been identified in countries throughout the world.
What are the common features of Williams syndrome?
Read detail for William Syndrome and William Syndrome children
