Williams Syndrome is a rare congenital disorder that occurs randomly and affects around one in 18,000 people in the UK. It is non-hereditary and causes ...

Williams syndrome, caused by a microdeletion on chromosome 7 (position 7q11.23), is a developmental condition characterised by mild to moderate intellectual ...

We are an information and advisory service with a register of UK cases of Williams Syndrome, supporting individuals with Williams Syndrome and those who love, ...

People with Williams syndrome can develop physical and mental health problems later in life, including anxiety and depression. People with Williams syndrome ...

It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges.

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

Williams syndrome is a rare congenital (present at birth) condition that is caused by missing genetic material from chromosome 7.

Williams syndrome is a rare genetic disorder, with a prevalence of between 1 in 7,500 and 1 in 20,000. It is caused by a deletion of approximately 21 genes on ...

Williams syndrome is a rare developmental disorder that can affect the heart and blood vessels. Learn more from Boston Children's Hospital.