Williams Syndrome Essay 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.
Amy Philofsky, in International Review of Research in Developmental Disabilities1 Williams Syndrome Overview Williams syndrome also called Williams-Beuren syndrome or Infantile Hypercalcemia is a neurodevelopmental, multisystem disorder associated with intellectual disability.
To date, 16 genes have been implicated in this region e. Nonetheless, the Williams syndrome phenotype is quite variable, with individuals evidencing a range of the common features and symptoms associated with the disorder.
During early development, individuals with Williams syndrome are at particular risk for certain serious physical conditions.
Vomiting, gastroesophageal reflux, and excessive irritability are common in infancy as well Francke, Amidst these complicated physical issues, individuals with Williams syndrome are also predisposed to show specific behavioral outcomes influencing cognitive, linguistic, social, and emotional development Bellugi et al.
Most individuals with Williams syndrome meet the clinical criteria for intellectual disability, but as they enter into middle childhood also show a complex profile of strengths in language and sociability and deficits in certain aspects of cognition.
In fact, individuals with Williams syndrome have been shown to perform better than typically developing MA matched controls on tests of verbal working memory, though differences are generally not significant Grant et al.
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. In particular, tasks that demand visuoconstructive abilities have been shown to be particularly impaired.William’s Syndrome (WS) or Williams-Beuren Syndrome (WBS) is a condition that is genetic in origin, is present at birth, and affects males and females equally.
Individuals with this syndrome have ongoing medical problems, which may include cardiovascular disease, developmental delays .
Williams Syndrome Lynamary Torres Chamberlain College of Nursing Pathophysiology II NR Summer, Williams Syndrome. Essays on Williams syndrome The Williams syndrome is one of the most popular assignments among students' documents.
If you are stuck with writing or missing ideas, scroll down and find inspiration in the best samples. Williams Syndrome Essay 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. Williams and Beuren published papers within months of each other in New Zealand and Germany.
Each described several patients with the same cardiovascular problem and a similar facial appearance. Williams syndrome is commonly used in the United States, while . Williams-Beuren syndrome (WBS) is a developmental disorder with multisystemic manifestations mainly characterised by vascular stenoses, distinctive craniofacial features, mental retardation with a characteristic neurocognitive profile, and some endocrine and connective tissue abnormalities, caused by a recurrent deletion of Mb including .