Williams Syndrome Index

Featured: Williams Syndrome Main Article

Williams syndrome is a developmental disorder that affects many parts of the body. Signs, symptoms, characteristics and features may include

  • intellectual disability,
  • learning problems,
  • unique personality characteristics,
  • distinctive facial features, and
  • heart and blood vessel problems.

Williams syndrome is a genetic condition that involves chromosome 7.

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Terms related to Williams Syndrome:

  • Beuren Syndrome
  • Elfin Facies Syndrome
  • Elfin Facies With Hypercalcemia
  • Hypercalcemia-Supravalvar Aortic Stenosis
  • Infantile Hypercalcemia
  • Supravalvar Aortic Stenosis Syndrome
  • WBS
  • Williams-Beuren Syndrome
  • WMS
  • WS