Williams syndrome

William Syndrome What is Williams Syndrome? The William syndrome is also known as WS, WMS and Williams-Beuren Syndrome (WBS). WS is an uncommon genetic disorder that is present at birth which can also affect females and males equally of any culture. The characteristic facial appearance and loving personality is what makes this rare syndrome to be unique. Most affected individuals with WS can have from mild to moderate retardation.According to the Williams Syndrome Association 20,000 people are affected

Williams syndrome is a rare, genetic disease affecting 1 out of 8,000 newborns (Williams syndrome, 2008). Caused by the deletion of several genes, there is no cure or treatment for it (Genetic Science Learning Center, 2014). While patients can live productive lives, they still face many difficulties in terms of their health and social skills. This condition is caused by the deletion of several genes located on the long arm (q arm) of at least one strand of chromosome 7. Some of these genes include

Williams Syndrome Williams Syndrome is a rare genetic disease that occurs at birth and can happen to just about anyone. Williams Syndrome is caused by a genetic deletion of parts of chromosome 7. The syndrome is commonly linked to causing a child to having a number of different learning and behavioral problems, such as a delay in growth, attention deficit disorder, and a number of learning disabilities. Williams Syndrome affects around 1 in 10,000 people worldwide, equally in both male and females

Williams Syndrome is a genetic condition that effects about one in every ten thousand people worldwide. While William Syndrome does effect learning, there is no disconnect in social interaction. People with WS tend to be very highly social people and play strong roles in their communities as adults. Although people with WS have strengths they also have many weaknesses. Babies often have life-threatening cardiovascular problems right at birth, and on many occasions they need ongoing medical care growing

For a student with Williams Syndrome they continue to fall behind with development and maturity behind their peers. Students begin to struggle with fitting in because their social skills are less appropriate. Their interests are not as varied as their peers which makes it a greater challenge socially. Students can have increased anxiety and depression and they “don’t understand why they’re different” (fact sheet). Students with Williams Syndrome have decreasing activity levels, but they continue

disorder that is known as Williams-Beuren Syndrome (Adams, 2012). This is often commonly referred to as something different when in fact it is the same disease. This refers to the names of the scientists that published papers at the same time researching the same disorder. Williams was a scientist from Australia and Beuren was from Germany (Prober, 2010). Williams is much more commonly used in the United States and Canada while the rest of the world normally uses Williams-Beuren as this is the more

Introduction Williams Syndrome(WS) is considered as a neurodevelopmental disorder, caused by a contiguous gene deletion of about 26 genes from the long arm of chromosome 7(Peoples et al., 2000). Since it had been first aware by J.C.P. Williams in 1961(Lenhoff, Wang, Greenberg & Bellugi, 1997), Williams Syndrome has drawn more attention in last 40 years. the incidence rate is approximately 1 in 2000 and diagnosed generally at 6.4 years old (Morris, Demsey, Leonard, Dilts & Blackburn, 1988). People

Since Williams Syndrome is a disorder characterized by the deletion of genes, treatments for this disease are very limited. There is no cure for this disease. There is no reprieve. There is no rest from the fact that the individual’s chromosome is missing over a megabyte of data (Meyer-Lindenberg, 2004). Due to the loss of elastin in the cardiovascular system, specifically in the heart, exercise is something that can be prescribed in order to prevent the arteries, veins, and chambers from collapsing

Williams Syndrome is a genetic disorder that happens in the fetus stage and after birth. This syndrome is caused by the deletion of 26-28 genes in chromosome 7. Symptoms include facial deformities, trouble speaking, and the narrowing of the Aorta with many more symptoms. This syndrome is tested at birth with fluorescent in situ hybridization or FISH. With blood samples, they test the blood for the deletion of chromosome 7. FISH checks if many as of 22-26 genes are deleted. Because there is no cure

Williams Syndrome Study: A Closer Look at Genetic Disease Introduction Genetic disorders offer a variety of different problems and symptoms. One of these disorders is Williams Syndrome. Williams syndrome is a genetic disorder characterized by the genetic alteration and deletion of genetic material on Chromosome 7 (Riby, 2008). This disorder can cause lack of mental functioning and have ill effects on health and other vital areas (Shiohama, 2016). Despite the drastic effects this alteration of