Mild to moderate intellectual disability is observed in people with WS, with particular challenges with.
Williams syndrome is caused by a microdeletion of at least 16 genes on chromosome 7q11. .
The educational profile for a student with Williams syndrome is a unique blend of strengths language and nonverbal reasoning and weakness in visuospatial construction (the ability to see an object or.
WHAT CAUSES WILLIAMS SYNDROME?.
Mar 27, 2023 · Williams syndrome (WS) is a rare genetic disorder. Jan 2, 2023 · Williams syndrome is an inherited genetic disorder that affects the development of children. In general, students with WS learn best.
. .  One study of 306 children with Williams.
Cognitive and developmental features may involve mild to severe learning disabilities and. The performance of twenty-eight individuals with Williams syndrome was compared with that of mental age- and gender-matched thirty-two typically developing children on tasks of learning of a visuo-motor sequence by.
This condition is characterized by mild to moderate intellectual disability or learning problems, certain personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems. .
. People with WS may have mild to moderate delays in their cognitive development (ability to think and reason) or learning difficulties.
Signs and symptoms include mild to moderate intellectual disability; unique personality traits; distinctive facial features; and heart and blood vessel problems.
. Educational Strategies. Language and face processing are seemingly spared, whereas other higher cognitive functions (spatial cognition, number, planning, and problem solving) are seriously impaired.
23. Williams syndrome is a genetic learning disability characterized by extreme language fluency and volubility, good awareness of appropriate body language and emotions. Signs and symptoms include mild to moderate intellectual disability; unique personality traits;. . . Learn about Williams Syndrome, including symptoms, causes, and treatments.
. Williams syndrome is a rare genetic disorder that causes a variety of symptoms and learning issues.
The performance of 16 individuals with Williams syndrome (six males, 10 females; mean age 18y 7mo [SD 7y 6mo], range 9y 1mo-30y 7mo) o Binding of visual and spatial short-term memory in Williams syndrome and moderate learning disability Dev Med Child Neurol.
Williams syndrome is a rare genetic condition which can give a person special facial features,.
Williams syndrome is caused by a person missing more than 25 genes from a specific area of chromosome 7 (a.
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.
Williams Syndrome is classified as an intellectual disability that can range from being mild to severe (Reynolds, Zupanick, & Dombeck, 2010).