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    Rett syndrome

    Rett syndrome is a disorder of the nervous system that leads to developmental reversals, especially in the areas of expressive language and hand use.


    Rett syndrome occurs almost always in girls. Itmay be misdiagnosed as autism or cerebral palsy.

    Studies have linked many Rett syndrome cases to a defect in a gene called methl-CpG-binding protein 2 (MeCP2). This gene is on the X chromosome. Females have two X chromosomes. Even when one chromosome has thisdefect, the other X chromosome is normal enough for the child to survive.

    Males born with this defective gene do not have a second X chromosome to make up for the problem. Therefore, the defect usually results in miscarriage, stillbirth, or very early death.

    The condition affects about 1 out of 10,000 children. Groups of the disease have appeared within families and certain areas of the world, including Norway, Sweden, and northern Italy.


    An infant with Rett syndrome usually has normal development for the first 6 - 18 months. Symptoms range from mild to severe.

    Symptoms may include:

    • Breathing problems -- problems tend to get worse with stress; breathing is usually normal during sleep and abnormal while awake
    • Change in development
    • Excessive saliva and drooling
    • Floppy arms and legs -- frequently the first sign
    • Intellectual disabilities and learning difficulties (assessing cognitive skills in those with Rett syndrome, however, is difficult because of the speech and hand motion abnormalities)
    • Scoliosis
    • Shaky, unsteady, or stiff gait; or toe walking
    • Seizures
    • Slowing head growth beginning at approximately 5 - 6 months of age
    • Loss of normal sleep patterns
    • Loss of purposeful hand movements; for example, the grasp used to pick up small objects is replaced by repetitive hand motions like hand wringing or constant placement of hands in mouth
    • Loss of social engagement
    • Ongoing, severe constipation and gastroesophageal reflux (GERD)
    • Poor circulation that can lead to cold and bluish arms and legs
    • Severe language development problems


    Problems in breathing pattern may be the most upsetting and difficult symptom for parents to watch. Why they happen and what to do about them is not well understood. Most experts in Rett syndrome recommend that parents remain calm through an episode of irregular breathing like breath holding. It may help to remind yourself that normal breathing always returns and that your child will become used to the abnormal breathing pattern.

    Exams and Tests

    Genetic testing may be done to look for the gene defect associated with the syndrome. However, since the defect is not identified in everyone with the disease, the diagnosis of Rett syndrome is based on symptoms.

    There are several different types of Rett syndrome:

    • Atypical
    • Classical (meets the diagnostic criteria)
    • Provisional (some symptoms appear between ages 1 and 3)

    Rett syndrome is classified as atypical if:

    • It begins early (soon after birth) or late (beyond 18 months of age, sometimes as late as 3 or 4 years old)
    • Speech and hand skill problems are mild
    • It is appears in a boy (very rare)


    Treatment may include:

    • Help with feeding and diapering
    • Methods to treat constipation and GERD
    • Physical therapy to help prevent hand problems
    • Weight bearing exercises for those with scoliosis

    Supplemental feedings can help those with slowed growth. A feeding tube may be needed if the child breathes in (aspirates) food. Diets high in calories and fat combined with feeding tubes can help increase weight and height. Weight gain may improve alertness and social interactions.

    Medications such as carbamazepine may be used to treat seizures. Other medications or supplements that have been used or studied include:

    • Bromocriptine
    • Dextromethorphan
    • Folate and betaine
    • L-carnitine, which may help improve language skills, muscle mass, alertness, energy and quality of life while decreasing constipation and daytime sleepiness
    • L-dopa for motor rigidity in later stages of the disease

    Stem cell therapy, alone or in combination with gene therapy, is another hopeful treatment.

    Support Groups

    International Rett Syndrome Association -

    Outlook (Prognosis)

    The disease slowly gets worse until the teenage years. Then, symptoms may improve. For example, seizures or breathing problems tend to lessen in late adolescence.

    Developmental regression or delays vary. Usually, a child with Rett syndrome sits up properly but may not crawl. For those who do crawl, many do so by scooting on their tummy without using their hands.

    Similarly, some children walk independently within the normal age range, while others are delayed, don't learn to walk independently at all, or don't learn to walk until late childhood or early adolescence. For those children who do learn to walk at the normal time, some keep that ability for their lifetime, while other children lose the skill.

    Life expectancies are not well studied, although survival at least until the mid-20s is likely. The average life expectancy of a girl with Rett syndrome may be mid-40s. Death is often related to seizure, aspiration pneumonia, malnutrition, and accidents.

    When to Contact a Medical Professional

    Call your health care provider if you:

    • Have any concerns about your child's development
    • Notice a lack of normal development with motor or language skills in a child
    • Think the child has a health problem that needs treatment


    The likelihood of having another child with Rett syndrome is less than 1%.


    Kwon JM. Miscellaneous Disorders. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 19th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 592.5.


          A Closer Look

            Self Care

              Tests for Rett syndrome

                Review Date: 11/12/2012

                Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine. Also reviewed by A.D.A.M. Health Solutions, Ebix, Inc., Editorial Team: David Zieve, MD, MHA, David R. Eltz, Stephanie Slon, and Nissi Wang.

                The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997- A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

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