Williams Syndrome

Synonyms

Aortic Stenoses, Hypercalcemia-Supravalvar

Aortic Stenosis, Hypercalcemia-Supravalvar

Beuren Syndrome

Chromosome 7q11.23 Deletion Syndrome

Contiguous Gene Syndrome, Williams

Hypercalcemia Supravalvar Aortic Stenosis

Hypercalcemia-Supravalvar Aortic Stenoses

Hypercalcemia-Supravalvar Aortic Stenosis

Stenoses, Hypercalcemia-Supravalvar Aortic

Stenosis, Hypercalcemia-Supravalvar Aortic

Supravalvar Aortic Stenosis Syndrome

Syndrome, Beuren

Syndrome, Williams

Syndrome, Williams-Beuren

Williams Beuren Syndrome

Williams Contiguous Gene Syndrome

Williams-Beuren Syndrome

A disorder caused by hemizygous microdeletion of about 28 genes on chromosome 7q11.23, including the ELASTIN gene. Clinical manifestations include SUPRAVALVULAR AORTIC STENOSIS; MENTAL RETARDATION; elfin facies; impaired visuospatial constructive abilities; and transient HYPERCALCEMIA in infancy. The condition affects both sexes, with onset at birth or in early infancy.