How Do You Teach A Child With Williams Syndrome?

What are elfin features?

Elfin facies is a form of facies where the patient presents with facial characteristics bearing some similarities to those traditionally associated with elves.

It is characterized by prominent forehead, widely spaced eyes, upturned nose, underdeveloped mandible, dental hypoplasia, and patulous lips..

How was Williams syndrome discovered?

Williams syndrome was first described by J. C. P. Williams and his colleagues, who wrote in 1961 of four patients with supravalvular aortic stenosis, mental disability, and facial features including a broad forehead, large chin, low-set, “drooping” cheeks, widely spaced eyes, and a wide-set mouth.

How do I know if my child has Williams syndrome?

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.

Why are people with Williams syndrome so happy?

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.

What is it like to have Williams syndrome?

Williams syndrome is a rare neurodevelopmental genetic disorder that features mild learning or developmental challenges, a high levels of calcium in the blood and urine, and a markedly outgoing personality. People with Williams syndrome (WS) often an unusual “elfin” appearance, with a low nasal bridge.

How can I help someone with Williams syndrome?

Treatment options for Williams syndrome There is no cure for Williams syndrome. Treatment involves easing the symptoms connected to the syndrome. Narrowed blood vessels can be treated if they cause symptoms. Physical therapy and speech therapy can also be beneficial.

Can Williams syndrome be cured?

Although there is no cure for Williams syndrome, it is important to identify and treat the different medical problems that can occur with this disorder. Treatments and interventions must be based on the unique needs of each individual.

Is Williams syndrome a form of autism?

Chris has Williams Syndrome (WS), a rare genetic disorder affecting around one in 18,000 people in Britain. It has often been dubbed the ‘opposite of autism’. People with WS are empathetic, social, friendly and endearing but they tend to have a low IQ, making tasks such as counting money difficult.

Does Williams syndrome run in families?

Is Williams syndrome inherited? Most cases of Williams syndrome are not inherited. The condition typically occurs due to random events during the formation egg or sperm cells in a parent. Therefore, it most often occurs in people with no family history of Williams syndrome.

Is Turner’s syndrome genetic?

Turner syndrome is not usually inherited in families. Turner syndrome occurs when one of the two X chromosomes normally found in women is missing or incomplete. Although the exact cause of Turner syndrome is not known, it appears to occur as a result of a random error during the formation of either the eggs or sperm.

How does Williams syndrome affect speech?

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.

Does Williams syndrome make you friendly?

Children with Williams syndrome tend to be social, friendly and endearing. Parents often say the joy and perspective a child with WS brings into their lives had been unimaginable. But there are major struggles as well. Many babies have life-threatening cardiovascular problems.

What is the life expectancy of someone with Williams syndrome?

Some people with Williams syndrome may have a reduced life expectancy due to complications of the disease (such as cardiovascular involvement). No studies specifically exist on life expectancy, although individuals have been reported to live into their 60s.

What is the difference between Down syndrome and Williams syndrome?

Williams syndrome is characterised by poor visuo-spatial abilities alongside relatively preserved language skills, whereas Down’s syndrome is characterised by lower language skills alongside less impaired visuo-spatial skills (e.g. Mervis and John, 2012).

What is Williams Beuren syndrome?

Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by growth delays before and after birth (prenatal and postnatal growth retardation), short stature, a varying degree of mental deficiency, and distinctive facial features that typically become more pronounced with age.

Are there any celebrities with Williams syndrome?

Lauren Taylor has Williams syndrome which means she’s unafraid of strangers.