Williams syndrome (WS) is a rare neurodevelopmental disorder characterized by:
a distinctive, "elfin" facial appearance, along with a low nasal bridge; an ...
Williams syndrome (WS) is a genetic condition that is present at birth and can
affect anyone. It is characterized by medical problems, including cardiovascular ...
Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic
disorder characterized by growth delays before and after birth (prenatal and ...
Sep 21, 2016 ... Williams syndrome is a genetic condition that causes various developmental and
health problems such as ADHD, anxiety, phobias, a short ...
Learn about Williams Syndrome, a very rare genetic disorder, from the Cleveland
Clinic, including causes, symptoms, diagnosis, treatment, and prognosis.
Jan 14, 2015 ... Originally described independently by Williams and Beuren in 1961, Williams
syndrome (WS) is a rare genetic condition. The clinical ...
Information on Williams syndrome, a condition that causes developmental delays
and medical problems throughout the body. Learn the causes, symptoms, ...
Williams Syndrome is named after a New Zealand cardiologist who, in 1956,
described a series of patients with very similar distinctive physical and intellectual
Jun 9, 2011 ... Williams Syndrome is a rare genetic condition -- so rare, in fact, that few people
have ever heard of it. Of about 7500 newborns, only one will ...
Sep 17, 2014 ... Williams syndrome, also known as WS, WMS, and Williams-Beuren syndrome (
WBS) is a rare neurodevelopmental genetic disorder in which ...