Genetic and hereditary syndromes

Williams Syndrome

Williams Syndrome is a rare genetic disorder caused by the deletion of genes on chromosome 7. It is characterised by distinctive facial feat...

About this profile

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.

Watch and listen

Williams Syndrome video 1
Williams Syndrome video 2

Common challenges

  • Difficulty with tasks requiring visual-spatial skills or fine motor coordination
  • Anxiety or social disinhibition in workplace interactions
  • Cardiovascular limitations affecting stamina and physical tasks
  • Sensitivity to loud noises or crowded environments
  • Trouble with multi-step tasks or abstract problem-solving

How to help

  • Match roles to verbal strengths and social abilities
  • Provide clear, step-by-step instructions and visual supports
  • Support cardiovascular-friendly pacing and workload planning
  • Educate employers on effective communication and social boundaries
  • Connect participants with vocational training that builds on strengths

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

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