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Williams Syndrome is a genetic condition that is evident from birth. It affects very many aspects of an individual’s functioning throughout life. Physical problems are numerous but among the most common are: cardiovascular and urinary tract abnormalities, hypertension, gastrointestinal complications, aching joints, mobility difficulties ...
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 distinctive facial characteristics and a wide range of learning difficulties.
Williams Syndrome is a genetically determined intellectually disabling condition. 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 one copy of chromosome 7.
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Adults and adolescents with Williams syndrome typically achieve a below-average height and weight, compared with unaffected populations. As people with WS age, they frequently develop joint limitations and hypertonia, or abnormally increased muscle tone.
Dec 10, 2021 · Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms including unique physical features, delayed development, cognitive challenges and cardiovascular abnormalities.
- Williams syndrome is a genetic condition characterized by unique facial features, delayed development, learning problems, and certain personality t...
- Williams syndrome is caused by a deletion, or missing piece, of a region on chromosome 7. Some important points to know about this genetic conditio...
- Williams syndrome may cause a range of developmental issues and symptoms. The condition is typically diagnosed in infancy or early childhood. Not a...
Jul 9, 2017 · Williams syndrome, also called Williams-Beuren syndrome, is a rare genetic disorder. It causes many developmental problems. These can include heart and blood vessel issues (including...
Jul 19, 2024 · What is Williams syndrome? 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) or learning difficulties.
