Exceptional social skills are also widely reported by those who work with children with Williams syndrome. Vomiting, gastroesophageal reflux, and excessive irritability are common in infancy as well Francke, Adults with Williams syndrome are typically limited in their ability to live independently or work in competitive employment settings, but this developmental impairment is attributed more to psychological symptoms than physiological problems.
Although WS participants started out at a lower performance level, TD and WS participants had a comparable amount of online and offline learning in terms of the accuracy of movement. Further advancements in technology allow individuals with communication difficulties to communicate through computer programs.
Unique personality traits include a high level of sociability and very good communication skills. The authors concluded that studies into WS could help scientists understand what it is that makes humans social beings.
Motor learning, particularly explicit learning of fine motor sequences has multiple phases.
Physical therapy can help to improve muscle tone, joint range of motion, and strength. These delays continue into childhood, where patients with Williams syndrome are delayed in learning to walk.
Offline consolidation is brain-state dependent: Individuals affected by Williams syndrome typically have high empathy, and are rarely observed displaying aggression.
Challenges faced by a person with WS include difficulty understanding spatial relations, abstract reasoning, and numbers, and some potentially life-threatening complications, such as Cardiovascular problems and a high level of calcium in the blood.
While verbal processing is an area of relative strength, visuospatial processing tends to be an area of relative weakness in Williams syndrome Mervis et al.
Cognitive and developmental features may involve mild to severe learning disabilities and cognitive challenges. Individuals with Williams syndrome who possess various forms of anxiety may benefit from cognitive behavioural therapy, which will help them isolate their fears and anxiety and give them methods in which to cope with these anxieties.
In addition, people with Williams syndrome often exhibit gross motor difficulties, including trouble walking down stairs, as well as overactive motor reflexes hyperreflexia and hyperactive, involuntary movement of the eyes nystagmus. In addition to post training sleep, sleep quality before learning also affects motor learning capacity in healthy individuals Williams syndrome (also called Williams-Beuren syndrome or Infantile Hypercalcemia) is a neurodevelopmental, multisystem disorder associated with intellectual disability.
Prevalence of Williams syndrome is estimated at approximately 1 in live births (Strømme, Bjornstad, & Ramstad, ). Williams Syndrome Essay - Williams Syndrome, also known as Williams-Beuren Syndrome, is a genetic disorder caused by a deletion along chromosome seven.
It is named for the two men who discovered and studied it inJ.C.P. Williams of the United States and A.J. Beuren of Germany. Williams syndrome also recognized as Williams-Beuren syndrome is a genetic disorder caused by a deletion of more than twenty five genes from chromosome 7.
Although Williams syndrome is often non-hereditary, the chances of the syndrome being passed on if an individual with Williams syndrome has a child are fifty percent. Williams Syndrome Essay Williams syndrome is a rare genetic disorder with a rate of incidence of approximately 1 in 20, births.
This usually results in mild to moderate mental retardation, although this is frequently accompanied by behavior patterns and abilities reminiscent of those of autistic savants. Williams syndrome also recognized as Williams-Beuren syndrome is a genetic disorder caused by a deletion of more than twenty five genes from chromosome 7 - Williams Syndrome introduction.
Although Williams syndrome is often non-hereditary, the chances of the syndrome being passed on if an individual with Williams syndrome has a child.
The syndrome was first described in by New Zealander John C. P. Williams. Williams syndrome affects between 1 in 7, to 1 in 20, people at birth. Life expectancy is less than that of the general population, mostly.Download