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 …

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 …

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 …

Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. WS occurs equally in males and females and in all cultures worldwide.

Williams syndrome is a genetic condition that affects many parts of the body. Signs and symptoms include mild to moderate intellectual disability; unique personality traits; distinctive …

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 …

Williams syndrome is an extremely rare genetic disorder that causes a range of cardiovascular issues, intellectual disabilities and facial differences.

Williams Syndrome (WS) is a rare genetic disorder characterized by mild to moderate delays in cognitive development or learning difficulties, a distinctive facial appearance, and a unique …

May 6, 2025 · Williams syndrome (WS; OMIM #194050 [1]), also known as Williams-Beuren syndrome, is a multisystem, contiguous gene deletion syndrome caused by hemizygous …

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, …