What is Williams Syndrome?
Williams syndrome is a genetic disorder that affects the development of the brain and body. It is most commonly seen in children, but can also occur in adults.
There are three main symptoms of Williams Syndrome: intellectual disability, facial features (such as a smaller nose or wide forehead), and heart problems.
The cause of Williams Syndrome is unknown, but it is believed to be caused by a combination of genes. Most people with Williams Syndrome have two copies of the gene for the disorder.
There is not currently any cure for Williams Syndrome, but there are treatments available that can help improve symptoms.
If you are concerned about your child’s development or if you think they may have Williams Syndrome, please talk to your doctor.
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