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Endocrine abnormalities: hypothyroidism, early puberty and diabetes in adulthood. . Cognitive and developmental features may involve mild to severe learning disabilities and.

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Cognitive and developmental features.

Signs and symptoms include mild to moderate intellectual disability; unique personality traits; distinctive facial features; and heart and blood vessel problems.

Williams syndrome is caused by a person missing more than 25 genes from a specific area of chromosome 7 (a. .

23. Symptoms of Williams syndrome include: Chronic ear infections and/or hearing loss.

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Williams syndrome is a developmental disorder that is characterized by cardiovascular problems, intellectual or learning disabilities, distinctive facial features, and a sociable personality.

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Jan 4, 2023 · Williams syndrome (WS) is a rare genetic condition characterized by high social interest and approach motivation as well as intellectual disability and anxiety. The syndrome appears due to a deletion of specific genes in chromosome 7. Williams syndrome is caused by a person missing more than 25 genes from a specific area of chromosome 7 (a. Signs and symptoms include mild to moderate intellectual disability; unique personality traits;. .

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WHAT CAUSES WILLIAMS SYNDROME?.

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