They have an extensive and interesting vocabulary and are often extremely interesting to converse with. Exceptional social skills are also widely reported by those who work with children with Williams syndrome.
Individuals with Williams syndrome often possess extremely varied strengths and weaknesses, and these strengths and weaknesses are not found in every single individual with Williams. Language abilities are at or slightly above the level expected for general cognitive ability.
For more Information If you are interested in finding out more about Williams syndrome, please visit the Williams Syndrome Association website. Many children with Williams syndrome can light up a room with their smiles and their positive approach to others.
Doris Kistler University of Louisville also collaborate on these studies. The elastin gene is not the only deletion on the seventh chromosome, but very little is known about what else has been affected.
Vomiting, Williams syndrome a genetic disorder psychology essay reflux, and excessive irritability are common in infancy as well Francke, Phobias, especially those involving certain loud or sudden noises, also are common.
Further advancements in technology allow individuals with communication difficulties to communicate through computer programs. Molecular genetics of Williams syndrome. Socio-communicative difficulties of children with Williams syndrome.
Material used to instruct a child or adolescent with Williams syndrome in an academic setting can be adapted as well, such as eliminating words or items on the page that are not important and limiting the number of math problems, or sentences within a page.
This project includes medical aspects of Williams syndrome as well as cognitive and behavioral aspects. 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.
The hemizygous deletion of the LIM-kinase1 gene contributes to the extreme difficulty individuals with Williams syndrome have with visuospatial construction.
Jeffrey Marler Ohio State University: People with Williams syndrome typically are limited in their general reasoning abilities.
Nonetheless, the Williams syndrome phenotype is quite variable, with individuals evidencing a range of the common features and symptoms associated with the disorder.
Williams syndrome is characterized by a distinctive pattern of cognitive strengths and weaknesses. Unsurprisingly, heart and circulatory problems are common in people with Williams syndrome, as is a higher than normal incidence of other problems involving internal organs.
The cerebellum, left frontal cortical and right parietal cortex regions are affected due to the deletion of genes, these abnormalities often cause behaviours such as an individual being hyper social.
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. The development of cardiovascular diseases and manifestations are one of the initial identifications of the syndrome, the most common cardiovascular abnormality is supravalvular aoetic stenosis, or SVAS for short, as mentioned before this disease is caused by the missing elastin gene.
Many individuals should be involved in the care of a person with Williams syndrome such as special education professionals, occupational and physical therapists, speech and language pathologists and general health professionals. This advanced language ability can also be repetitive and unfocused, and some people with Williams are nonverbal.
Neuroimaging studies of children and adults with Williams syndrome who have normal intelligence. At the University of Louisville, we collaborate with Dr. This article includes suggestions for speech and language intervention. An infant will often have a low birth weight and have difficulty when it comes to eating; which later causes the baby to grow at a slower pace than is considered normal.
Research on Williams syndrome is in its infancy, but it will surely become much better understood over time.Williams syndrome Williams-Beuren syndrome (WBS) is a multisystem disorder with an incidence of 1 in 20, births and is caused by a microdeletion on. 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 Essay 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 are fifty percent. What is Williams syndrome? Williams syndrome is a developmental disorder caused by a microdeletion on the long arm of chromosome 7.
This deletion encompasses ~25 genes, including Elastin and LIM-kinase1. Many individuals with Williams syndrome have congenital heart defects such as supravalvar aortic stenosis (SVAS), hernias, and/or other connective tissue disorders. 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 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 is a rare genetic disorder which leads to developmental problems, such as: a child’s growth, physical appearance and cognitive development.
This syndrome is .Download