williams syndrome - Axtarish в Google
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Mild to moderate intellectual disability is observed, particularly challenges with visual spatial tasks such as drawing. Verbal skills are relatively unaffected ...
Синдром Вильямса
Синдром Уильямса — синдром, возникающий как следствие наследственной хромосомной перестройки. Люди, страдающие этим синдромом, обладают специфической внешностью и характеризуются общей задержкой умственного развития при развитости некоторых... Википедия
МКБ-10 : Q93.8
МКБ-9 : 758.9
OMIM : 194050
Williams syndrome is a rare genetic condition characterized by physical traits, cognitive delays and heart abnormalities.
31 мая 2022 г. · Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate ...
It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges. These often occur side by side with ...
13 апр. 2023 г. · Williams syndrome (WS) is characterized by developmental delay, intellectual disability (usually mild), a specific cognitive profile, ...
Williams syndrome is a rare genetic condition. It is characterised by distinctive physical features and behaviours, including a distinctive facial appearance, ...
Williams syndrome is a rare developmental disorder that can affect the heart and blood vessels. Learn more from Boston Children's Hospital.
Causes. Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. ... One of the missing genes is the gene that produces elastin.
Learn about Williams Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find ...
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