Most children with Williams syndrome do not require any special diet, but may be on a reduced calcium diet. A well-balanced diet and exercise is important to reduce the risk of diabetes. Gastroesophageal reflux may be present. Chronic constipation is common.
Sucking, swallowing and chewing problems can all disrupt the ability of the child to eat and thus take away the ability to find pleasure in eating. It is important to prevent or manage these difficulties from birth as they can have an impact on the development of oral abilities, both nutritional and verbal.
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.
Children with WS tend to be thin. Sometimes adults with WS are also thin, but some adults may gain weight, especially in their belly, hips or legs. It is healthy and normal for everyone to have some body fat, including those with and without WS.
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.
Despite the possibility of medical problems, most children and adults with Williams syndrome are healthy and lead active, full lives.
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.
Dental abnormalities include malocclusion, hypodontia, malformed teeth, taurodontism, pulp stones, increased space between teeth, enamel hypoplasia, and high prevalence of dental caries.
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.
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.
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.
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 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.
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.
Elastin is an important part of elastic fibers found in the connective tissue of many organs. The missing elastic explains some of the characteristics of WS, such as certain facial features, hoarse voice, bladder and bowel diverticula, heart problems, and joint problems.
The most significant medical problem that occurs with WS is cardiovascular (heart) disease caused by narrowed arteries. Infants with WS may also have elevated levels of blood calcium. Clinical trials are studies that allow us to learn more about disorders and improve care.
Research studies have suggested that IQ scores for children with Williams syndrome range from 40 to 112, with a mean IQ score of 68 which equates to a mild intellectual disability (average IQ is 100). However, it has been reported that in individuals with smaller genetic deletions IQ scores may be higher.
The personality of individuals with Williams syndrome involves high sociability, overfriendliness, and empathy, with an undercurrent of anxiety related to social situations.
Older children and adults with Williams syndrome may develop progressive joint problems that limit their range of motion.
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.
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.
Causes. Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. In most cases, the gene changes (mutations) occur on their own, either in the sperm or egg that a baby develops from.
3) Use simple, concrete language at all times. Avoid complex and abstract explanations or concepts. 4) Remember that the person with Williams Syndrome usually understands less than may be apparent from the way they talk.
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.
Pober says few people with William's syndrome marry, and even fewer have children. But this may be changing, Pober says.