Williams syndrome (WS), also known as Williams–Beuren syndrome (WBS), is a
rare neurodevelopmental disorder characterized by: a distinctive, "elfin" facial ...
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 is a developmental disorder that affects many parts of the
body. This condition is characterized by mild to moderate intellectual disability or
Williams syndrome is a genetic condition that causes various developmental and
health problems. Read more about the symptoms, genes, and diseases ...
Aug 4, 2015 ... Williams syndrome, also called Williams-Beuren syndrome, is a rare genetic
disorder that causes multiple developmental problems. This can ...
Williams syndrome is a rare genetic disorder that affects a child's growth, physical
appearance, and cognitive development. People who have Williams ...
Jan 14, 2015 ... Originally described independently by Williams and Beuren in 1961, Williams
syndrome (WS) is a rare genetic condition. The clinical ...
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 ...
Comprehensive information and resources regarding Williams syndrome.
Williams Syndrome Changing Lives Foundation understanding Williams
Williams Syndrome occurs in about one per 7,500 to 20,000 births. It is also
known as Beuren Syndrome, Williams-Beuren Syndrome, WBS, WMS, and ...