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%.
One of the characteristics of Williams syndrome is an inappropriate increase in social behavior.
Abnormally high blood pressure (hypertension) is also common in adults with this disorder. Children with Williams syndrome typically have a personality that is friendly, outgoing, and/or talkative. The appropriate use of language and vocabulary range may be unusually enhanced in some children with this disorder.
Individuals with WS typically demonstrate an overly friendly, affectionate, engaging, and socially disinhibited personality [6, 12].
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 ...
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 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.
They may have a unique ability to connect with others and form strong bonds, making them appear very happy and engaging. Additionally, people with Williams syndrome often have a keen interest in music. They may have a talent for it, contributing to their overall well-being and happiness.
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.
The Williams Syndrome Association also has special growth charts for children with Williams syndrome as well as guidelines for administering anesthesia and for health transition to adulthood in their medical resources. Williams syndrome itself does not get worse over time.
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.
The face and mouth of someone with Williams syndrome may show: A flattened nasal bridge with small upturned nose. Long ridges in the skin that run from the nose to the upper lip. Prominent lips with an open mouth.
Despite the possibility of medical problems, most children and adults with Williams syndrome are healthy and lead active, full lives.
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.
Cardiovascular defects are the most common cause of death in patients with WS.
Patients usually have a normal life expectancy. Some patients may have a reduced life expectancy. This is due to complications related to the heart and kidney. There is no cure for Williams syndrome.
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.
Williams Syndrome (WS) is a genetic disorder associated with mental retardation (MR) and a distinct behavioral phenotype including a friendly and outgoing personality.
Williams Syndrome is a rare congenital disorder that occurs randomly and affects around one in 18,000 people in the UK. It is non-hereditary and causes distinctive facial characteristics and a wide range of learning difficulties.
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).
Williams syndrome is a progressive disorder with multisystem involvement.
Williams syndrome is usually diagnosed before a child is 4 years old. Your doctor will do an exam and ask about your family medical history. Then the doctor will look for facial features like an upturned nose, wide forehead, and small teeth. An electrocardiogram (EKG) or ultrasound can check for heart problems.
Parents of 57 of the 96 children (59.4%) indicated that their child had difficulty falling asleep. Thirteen children (out of 95, 13.7%) were reported to wake up more than twice per night and 26 (out of 95, 27.4%) had difficulty falling back asleep if they woke up at night.