As well as a learning disability, people with Williams syndrome will often share distinctive facial characteristics including a wide mouth with a pronounced bottom lip, slightly high and rounded cheeks, and widely-spaced teeth.
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.
Williams syndrome is a lifelong condition; it cannot be cured. It causes learning disabilities, certain distinctive facial features, and an increased likelihood of developing certain health issues, such as heart problems.
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.
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.
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) is not an autism spectrum disorder (ASD), although there is some overlap between the two conditions. WS and ASD have opposite characteristics in the social domain, but share some common behavioral and cognitive deficiencies.
Yes, but the number and the severity of problems varies greatly among individuals. Many different body systems can be affected and since some of the medical problems can develop over time, it is important that individuals with Williams syndrome receive ongoing medical monitoring and supervision.
Williams syndrome may cause poor growth in childhood, and most adults with the condition are shorter than average. Williams syndrome can also cause endocrine concerns like having too much calcium in your blood and urine, an underactive thyroid and early puberty.
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.
In general, students with Williams syndrome learn best with consistency, structured instructional routines, clear and realistic expectations, social stories, scripts and visual schedules, and technology. In particular, students with WS are often very effective users of computers and iPads/tablets.
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.
The personality of individuals with Williams syndrome involves high sociability, overfriendliness, and empathy, with an undercurrent of anxiety related to social situations.
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.
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.
Williams syndrome is a progressive disorder with multisystem involvement.
There is little evidence for self-injury in Williams syndrome. Several studies have examined aggression in Williams syndrome and a review of aggression is far less common in Williams syndrome (6-15%) compared to other syndromes such as Smith-Magenis, Prader-Willi and Angelman syndromes, who all have rates over 70%.
The behavioral symptoms of the syndrome include over-friendliness, increased empathy (the ability to understand the feelings of others), cognitive (mental) disorders, highly developed language skills, disrupted ability to recognize danger in social situations, and high levels of non-social stress (stress that is not ...
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].
Can people with Williams Syndrome have a child/children of their own? There are no significant physical reasons why people with Williams Syndrome cannot conceive normally, but their own health may pose a potential risk, particularly if they have a heart condition.
Williams syndrome (WBS) is a genetic multisystem disorder. The main symptom is borderline (intelligence quotient, IQ 70–79) or abnormally low intelligence (IQ < 70).
Williams syndrome (WS) is a genetic developmental disorder that affects many parts of the body, including the brain, heart, blood vessels, and facial features. The syndrome often causes brain-related symptoms such as intellectual disabilities, cognitive impairments, behavioral issues, and specific personality traits.
Communication difficulties: Most children with Williams syndrome develop speech skills later than other children their age. With intervention, most children develop the ability to communicate wants and needs effectively. In fact, for many children with Williams syndrome, expressive language may be a relative strength.
What causes Williams syndrome? Williams syndrome is caused by a partial deletion of up to 28 genes on chromosome 7. This means that a section of genetic material on chromosome 7 is missing. It is believed that some of these genes are involved in the production of elastin.