ABOUT THE SYNDROME

Williams syndrome is a rare genetic condition (estimated to occur in 1/7,500 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.

Below you will find a set of questions and advice gathered from various sources (other associations in other countries, parents - Romanians or foreigners, professional articles). The sources are mentioned at the end of every article/paragraph. 


1. Which are the most common characteristics of Williams Syndrome ?

2. Guidelines for parents/caregivers of persons with Williams Syndrome.

3. Medical information