Williams syndrome


Wil·liams syndrome

noun \ˈwil-yəmz-\

Definition of WILLIAMS SYNDROME

:  a rare genetic disorder marked especially by hypercalcemia of infants, heart defects, characteristic facial abnormalities, and mild to moderate mental retardation but a high verbal aptitude

Origin of WILLIAMS SYNDROME

J. C. P. Williams b1922 New Zealand physician
First Known Use: 1981

Wil·liams syndrome

noun \ˈwil-yəmz-\   (Medical Dictionary)

Medical Definition of WILLIAMS SYNDROME

: a rare genetic disorder characterized especially by hypercalcemia of infants, heart defects (as supravalvular aortic stenosis), characteristic facial features (as an upturned nose, long philtrum, wide mouth, full lips, and pointed chin), a sociable personality, and a high verbal aptitude, but with mild to moderate mental retardation

Biographical Note for WILLIAMS SYNDROME

Williams, J. C. P. (flourished 1961), New Zealand cardiologist. Williams was the principal author on a 1961 article on supravalvular aortic stenosis, with B. G. Barratt-Boyes and J. B. Lowe listed as secondary authors.

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