Williams syndrome is a rare genetic disorder that is caused by the deletion of genetic material on
Behavioural difficulties include: lack of social inhibition/discrimination, attention deficits, fears phobias, generalized anxiety (often related to health and illness), preoccupations obsessions (e.g. certain types of machinery e.g. lawn mowers, washing machines) and perseverative behaviour (doing or saying the same ...
Individuals with WS often have a personality and behavior pattern that includes distractibility, restlessness, social disinhibition, excessive talking, mood swings and anxiety [8], the latter of which is one of the most distinguishable features of this behavioral phenotype [5].
The key dimensions of WS sociability include increased approachability, attention to faces, and emotional responsivity.
Williams syndrome (WS) is a rare genetic syndrome (prevalence 1: 75001) characterized by strikingly heightened social approach behaviors. Individuals with WS are typically described as “hypersocial”, with a strong social interest, friendliness, and attention to other's2,3,4,5,6.
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.
Often, children with Williams syndrome have strong verbal and communication skills, which could mask delays to their cognitive abilities, which are common in Williams syndrome-like learning numbers and letters, differentiating between real and abstract and their ability to understand the space between objects.
Individuals with Williams syndrome tend to have difficulty with visual-motor skills and visuospatial construction. They also have difficulties with maths and in maintaining focus more generally. This distractibility is very common during mid-childhood, but tends to become less of a problem as children grown older.
Even claims about very low IQ turn out to be exaggerated. Williams syndrome IQ ranges from 48 to 85. True, people with Williams syndrome are often very loquacious and usually have better language than spatial skills, but the profile of the syndrome is unscientifically exaggerated by secondary sources.
It affects approximately 1 in 10000 Australians. There are many symptoms that vary from person to person, but they each share a very social and friendly disposition and have a deep affinity with music.
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.
Your physician should follow the guidelines provided by the American Medical Association. Despite the possibility of medical problems, most children and adults with Williams syndrome are healthy and lead active, full lives.
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 often goes undiagnosed. This means many people fail to get the support and treatment they need until later in life. Diagnostic tests include: medical history.
Anxiety is a prevalent mental health issue for individuals with Williams syndrome (WS). Relatively little is known about the developmental course of anxiety, or how it links with core features of WS, namely social and executive functioning (EF).
And they found that people with Williams syndrome have a lot more oxytocin than everybody else, and that it fluctuates wildly in the brain. As a result, they feel this biological impulse to love all the time.
Williams Syndrome (WS) is a genetic disorder associated with mental retardation (MR) and a distinct behavioral phenotype including a friendly and outgoing personality.
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.
Strengths in speech, long term memory, and social skills. Weaknesses in fine motor and spatial relations. Movement/mobility difficulties: Most children with Williams syndrome have low muscle tone and trouble with coordination and strength. Young children may be slow in developing motor skills.
Most patients with Williams syndrome are diagnosed as a newborn or in early childhood. The average age of diagnosis is around three and a half years.
Most individuals with Williams syndrome have an affinity to music. They are touched by music in ways not usually seen in the general population.
Williams syndrome is a progressive disorder with multisystem involvement.
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.
Beyond infancy, findings have consistently indicated that children with WS have more sleep problems than age-matched TD children, including sleep anxiety, bedtime resistance, sleep onset delay, frequent night waking, general restlessness, and excessive daytime sleepiness [10, 11, 41,42,43,44,45,46,47].
Children with Williams syndrome frequently present with symptoms of attention deficit hyperactivity disorder (ADHD), but there is little information that stimulant medication is useful in this population.