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  1. Since the last review of Williams syndrome in Current Opinion (2001) there have been many advances in knowledge about the cognitive, social and psychological impairments that characterize the disorder. The present review focuses on current research in these areas. Recent findings.

  2. 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.

  3. Williams syndrome (WS) is a rare genetic disorder that occurs 1 in 18,000 live births and is caused by a genetic deletion on the long arm of chromosome 7. Individuals with WS often show uneven cognitive profiles with better language abilities, compared to non-verbal or visuo-spatial abilities.

  4. www.mencap.org.uk › learning-disability-explainedWilliams Syndrome | Mencap

    • What Is Williams Syndrome?
    • Williams Syndrome and Learning Disability
    • How Does Williams Syndrome Affect someone?

    Williams syndrome is a rare genetic condition. It occurs randomly and affects 1 in 18,000 people in the UK. Williams syndrome is notpassed on from parent to child.

    Williams syndrome affects everyone in different ways, but many people will have a learning disability A learning disability is to do with the way someone's brain works. It makes it harder for someone to learn, understand or do things. . A child's development will be delayed if they have Williams syndrome, which means they may take longer to learn h...

    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. People with Williams syndrome can develop physical and mental health problems later in life, including anxiety and depress...

  5. To celebrate the 40th anniversary of the Williams Syndrome Foundation and to raise awareness of Williams syndrome, we have put together 40 research-evidenced facts about Williams syndrome. Williams Syndrome is a rare genetic condition that is caused by a deletion of genetic material on the long arm of chromosome 7.

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  7. Oct 1, 2011 · Williams syndrome (WS) is a rare genetic disorder characterized by heart disease, failure to thrive, hearing loss, intellectual or learning disability, speech and language delay,...

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