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- DictionaryWilliams/ˈwɪljəmz/
noun
- 1. a dessert pear of an early green variety.
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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. Infants often have delayed development and can develop physical and mental health problems, including anxiety and ...
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Williams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges. These often occur side by side with striking verbal abilities, highly social personalities, and an affinity for music.
Williams syndrome is caused by a tiny piece of information in a chromosome missing. A simple blood test can tell if a chromosome is different to normal, which can help towards getting a diagnosis. Early diagnosis can help you get the support you need, so make sure you contact a GP if you are worried.
Apr 7, 2014 · 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. They ...
20.IndividualswithWilliamsSyndromecanhaveweakcentralcoherence, whichmeanstheyseethingsdifferentlytootherpeople.For example,peoplewithWilliamsSyndromemaybemorelikelytolook
Sep 22, 2024 · Williams syndrome is a rare genetic disorder caused by a missing section of a chromosome. It causes unique facial features, physical symptoms, cognitive delays, and learning differences.
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th 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. It occurs sporadically in about 1 in 18,000 people.
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