URL of this page: https://www.nlm.nih.gov/medlineplus/rettsyndrome.html

Rett Syndrome

Summary

Rett syndrome is a rare genetic disease that causes developmental and nervous system problems, mostly in girls. It's related to autism spectrum disorder. Babies with Rett syndrome seem to grow and develop normally at first. Between 3 months and 3 years of age, though, they stop developing and even lose some skills. Symptoms include

  • Loss of speech
  • Loss of hand movements such as grasping
  • Compulsive movements such as hand wringing
  • Balance problems
  • Breathing problems
  • Behavior problems
  • Learning problems or intellectual disability

Rett syndrome has no cure. You can treat some of the symptoms with medicines, surgery, and physical and speech therapy. Most people with Rett syndrome live into middle age and beyond. They will usually need care throughout their lives.

NIH: National Institute of Child Health and Human Development

Start Here

  • Rett Syndrome (Mayo Foundation for Medical Education and Research)
  • Rett Syndrome From the National Institutes of Health (National Institute of Child Health and Human Development)
  • Rett Syndrome From the National Institutes of Health (National Institute of Child Health and Human Development)
  • Rett Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke) Available in Spanish
  • Rett Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke) - Short Summary

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