The Williams Syndrome Center at St. Louis Children's Hospital offers coordinated care for the diagnosis and treatment of Williams syndrome (WS). Williams syndrome is a rare genetic disorder that is associated with developmental delays and medical problems affecting multiple parts of the body.
Features of Williams syndrome include:
- Facial features often described as pixie-like
- Feeding problems
- Developmental delays
- Characteristic personality features
- Blood vessel and other heart problems
- Problems with hormones
Additional health concerns associated with Williams syndrome include:
- Eye crossing
- Difficulty with potty training: increased frequency of needing to go to the bathroom, urgency leading to accidents, or the feeling of pain with urination
- Hernias and other problems related to connective tissue, such as loose or tight joints
Why Choose the Williams Syndrome Center?
The health issues that accompany Williams syndrome are not one size fits all. That’s why it’s important to be treated at a center with a team of specialists who have expertise in Williams syndrome — so that your child gets the individual treatment plan that best fits his or her needs. Our team is here to help you each step of the way — from which therapies to provide for your child now to what to watch for as your child develops.Learn More
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