williams syndrome infant - Axtarish в Google
Description. Williams syndrome is a developmental disorder that affects many parts of the body . This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems.
31 мая 2022 г.
Williams syndrome is a disorder that causes developmental delays, learning problems (like trouble with space and numbers), and heart and blood vessel ...
Williams syndrome is a rare genetic condition characterized by unique physical features, delays in cognitive development and potential cardiovascular ...
Personality traits including being very friendly, trusting strangers, fearing loud sounds or physical contact, and being interested in music; Short height, ...
Williams syndrome is a rare developmental disorder that can affect the heart and blood vessels. Learn more from Boston Children's Hospital.
22 сент. 2024 г. · Williams syndrome is a rare genetic disorder that can cause physical, cognitive, and cardiovascular problems.
Most patients with Williams syndrome are diagnosed as a newborn or in early childhood. The average age of diagnosis is around three and a half years. Not all ...
14 окт. 2024 г. · Williams syndrome happens when a gene that's usually found on chromosome 7 is missing. In most cases, this genetic change happens by chance.
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 ( ...
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