Williams syndrome was first described by J. C. P. Williams and his colleagues, who wrote in 1961 of four patients with supravalvular aortic stenosis, mental disability, and facial features including a broad …

Dec 10, 2021 · What is Williams syndrome? Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms …

Apr 9, 1999 · Williams syndrome (WS) is characterized by developmental delay, intellectual disability (usually mild), a specific cognitive profile, unique personality characteristics, cardiovascular disease …

Sep 22, 2024 · Williams syndrome (WS), also called Williams-Beuren syndrome (WBS), is a rare genetic disorder that causes a variety of symptoms throughout the body. If your child's been diagnosed with...

Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, including cardiovascular disease, developmental delays, and …

Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality …

Williams syndrome (WS; OMIM #194050 [1]), also known as Williams-Beuren syndrome, is a multisystem, contiguous gene deletion syndrome caused by hemizygous deletion of 1.5 to 1.8 Mb on …

What is Williams syndrome? Williams syndrome is a genetic condition that affects the body’s typical growth and development. It can affect many parts of the body, including the heart and blood vessels.

Jan 14, 2015 · What Is Williams Syndrome? Williams syndrome (also termed Williams-Beuren syndrome) is a rare genetic disorder (in chromosome 7) that results in prenatal and postnatal growth …

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 …