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Williams Syndrome At a Glance

picture courtesy of the Williams Syndrome Association 

Print a PDF of all Williams Syndrome information.

Williams syndrome (WS) is a genetic condition characterized by heart, facial and personality differences and often accompanied by mild to moderate intellectual disability. It is caused by missing material, called a microdeletion, on chromosome 7. This missing piece disrupts the gene that helps make elastin.  Elastin is a protein that gives elasticity to our tissues and organs.  It is found in the walls of arteries, and in the lungs, intestines, and skin.  Reduced or abnormal elastin may explain the physical, medical, and facial differences seen in Williams syndrome.

About one in every 7,500 babies is born with Williams syndrome. 

Click here to read about symptoms that may be associated with Williams syndrome. Note: There is wide variability within individuals who have this condition. 

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