Williams syndrome is caused by a genetic abnormality, specifically a deletion of about 27 genes from the long arm of one of the two chromosome 7s. ... Typically, ... Gabrielle Marion-Rivard · Syndromic autism · Chromosome 7 |
| 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
31 мая 2022 г. · This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, ... |
1 мая 2008 г. · Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by growth delays before and after birth ( ... |
Williams syndrome is a rare genetic condition. It is characterised by distinctive physical features and behaviours, including a distinctive facial appearance. |
31 дек. 2023 г. · 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. |
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