About
Williams Syndrome is a rare genetic disorder caused by the deletion of genes on chromosome 7. It is characterised by distinctive facial features, cardiovascular issues (e.g., supravalvular aortic stenosis), developmental delays, and a unique cognitive profile with strong verbal skills but challenges in spatial reasoning and fine motor tasks.
This condition is often invisible.
Many disabilities, including this one, may not have outward signs—people can be significantly impacted even if they appear “fine” on the outside.
Common Challenges
Practitioner Help
Common Accommodations
Notes
Williams Syndrome presents a mix of strengths and challenges. Leveraging verbal abilities while providing structured support for spatial tasks and sensory sensitivities helps individuals succeed in the workplace.
May is Williams Syndrome Awareness Month