Williams syndrome is a rare genetic condition characterized by physical traits, cognitive delays and heart abnormalities.

Williams syndrome is caused by a partial deletion of up to 28 genes on chromosome 7. This means that a section of genetic material on chromosome 7 is missing. Symptoms of Williams syndrome · What causes Williams...

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. This is ...

Williams syndrome is caused by a change in the amount of an individual's genetic make-up, or DNA. DNA is found in the form of structures called chromosomes.

It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges. These often occur side by side with ...

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, ...

22 сент. 2024 г. · Williams syndrome is a rare genetic disorder that can cause physical, cognitive, and cardiovascular problems.

Cause:This disease is caused by changes to the number or structure of a person's chromosomes. Organizations:Patient organizations are available to help find a ...

7 авг. 2024 г. · A higher frequency of obesity, impaired glucose tolerance, and diabetes mellitus have been found in adults with Williams syndrome compared to ...