Williams Syndrome is a rare genetic condition that is caused by a deletion of genetic material on the long arm of chromosome 7. It occurs sporadically in ...

Williams Syndrome (WS) is a rare genetic disorder characterized by mild to moderate delays in cognitive development or learning difficulties.

Williams syndrome is caused by the spontaneous deletion of 26-28 genes on chromosome #7 at the time of conception.

Williams syndrome is a rare genetic condition characterized by unique physical features, delays in cognitive development and potential cardiovascular problems.

19 июл. 2024 г. · Williams syndrome (WS) is a rare genetic disorder. People with WS may have mild to moderate delays in their cognitive development (ability to think and reason) ...

31 мая 2022 г. · Young children with Williams syndrome have distinctive facial features including a broad forehead, puffiness around the eyes, a flat bridge of ...

Williams syndrome is a rare genetic condition. It is characterised by distinctive physical features and behaviours, including a distinctive facial appearance. Symptoms of Williams syndrome · What causes Williams...

7 мая 2019 г. · Below you will find some interesting facts ... The most common symptoms of Williams Syndrome includes unusual facial features and heart defects.

Children who have Williams syndrome often have mild-to-moderate intellectual disability, distinctive facial features, and certain behavioral characteristics ...

WS affects 1 in 10,000 people worldwide – an estimated 20,000 to 30,000 people in the United States. It is known to occur equally in both males and females and ... Personal Stories of WS · What is WS · Our Team · Diagnosis