Older children and adults with Williams syndrome may develop progressive joint problems that limit their range of motion.
Although hyperactivity may reduce in adults, persistent distractibility is still noted for many. Adults with Williams syndrome may also be less eager to learn than children with Williams syndrome. Anxiety tends to persist with age and adults may acquire additional fears and phobias over time.
Consider the progressive nature of medical problems in Williams syndrome, including vascular stenosis, hypertension, and joint contractures. Medical complications may occur, especially related to the cardiovascular system. However, most individuals with Williams syndrome are healthy and lead active full lives.
Most people with Williams syndrome have a normal life expectancy, but some may have a reduced life expectancy due to complications of the disease (such as cardiovascular problems).
Despite the possibility of medical problems, most children and adults with Williams syndrome are healthy and lead active, full lives.
What is Williams syndrome? Williams syndrome (WS) is a rare genetic disorder. People with WS may have mild to moderate delays in their cognitive development (ability to think and reason) or learning difficulties.
Cardiovascular defects are the most common cause of death in patients with WS.
Description. Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems.
The personality of individuals with Williams syndrome involves high sociability, overfriendliness, and empathy, with an undercurrent of anxiety related to social situations.
Williams syndrome is a rare genetic disorder that is caused by the deletion of genetic material on chromosome 7. Typical characteristics include distinctive facial features, mild intellectual disability and an overly sociable personality.
Williams syndrome is called the happy syndrome because people with this condition often have outgoing, friendly personalities and tend to be very social. They may have a unique ability to connect with others and form strong bonds, making them appear very happy and engaging.
Williams syndrome is a spectrum disorder. There is a great deal of variability in individuals throughout the spectrum. Medical concerns and learning challenges, emotional issues, and anxiety are common and can be all-consuming at times. The severity of the challenges varies and can ebb and flow over the years.
Driven To Trust. Jessica's daughter, Isabelle, has Williams syndrome, a genetic disorder with a number of symptoms. Children with Williams are often physically small and frequently have developmental delays. But also, kids and adults with Williams love people, and they are literally pathologically trusting.
Anxiety is thought to affect between 60-90% of individuals with Williams syndrome. Mood regulation problems are also very common and often occur with ADHD, anxiety and sensory modulation difficulties.
Williams syndrome (WS; also known as Williams–Beuren syndrome; OMIM 194050), is a distinctive multisystem disorder (Figure 1, Supplementary box 1). The most common areas of involvement include the cardiovascular, central nervous, gastrointestinal and endocrine systems, although any organ system could be affected.
Autism and Williams syndrome are genetically based neurodevelopmental disorders that present strikingly different social phenotypes. Autism involves fundamental impairments in social reciprocity and communication, whereas people with Williams syndrome are highly sociable and engaging.
Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks.
The low I.Q., however, ignores two traits that define Williams more distinctly than do its deficits: an exuberant gregariousness and near-normal language skills. Williams people talk a lot, and they talk with pretty much anyone [p.
Although low mood in Williams syndrome is less well researched, there are indications that clinical depression diagnoses may be present in approximately 10% of individuals.
One of the characteristics of Williams syndrome is an inappropriate increase in social behavior. People with the syndrome may be overly friendly, even to strangers.
Our own research has shown that children with WS generally have a very limited vocabulary up until the mental age1 of 18 months and many children may not say their first word until they are older than two years. There are a number of reasons why language abilities may be delayed in WS.
Scientists realized it was related to the levels of oxytocin. They knew that oxytocin is involved in social/intimacy behaviors, like mother-child bonding or romantic encounters. And they found that people with Williams syndrome have a lot more oxytocin than everybody else, and that it fluctuates wildly in the brain.
The premature ageing of organs caused by the condition can mean that a person with Williams Syndrome, whilst able to enjoy a relatively long and healthy life, might not have the same life expectancy as a person without Williams Syndrome.