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Rett syndrome





Rett syndrome

Treatment:



Treatment may include:

  • Supportive care (assistance with feeding, diapering, and treating symptoms like constipation and GERD).
  • Supplemental feeding for those with slowed growth. Diets high in calores and fat, as well as nasogastric tube feeds, can help increase weight and height. Weight gain, in turn, may improve alertness and social interactions. If the person with Rett syndrome is prone to breathing in food, a feeding tube into the stomach may be recommended.
  • Physical therapy for the hands to prevent them from contracting. Also, weight bearing exercises and frequent followup are recommended for those with scoliosis.
  • Medication, like carbamazepine, to treat seizures.

Other medications or supplements that have been used or studied include:

  • L-dopa for motor rigidity in later stages of the disease
  • L-carnitine -- some families report improvement in language skills, increased muscle mass, decreased constipation, increased alertness, less daytime sleeping, increased energy, and improved quality of life while their daughters took carnitine
  • Folate and betaine
  • Dextromethorphan
  • Bromocriptine

Given the discovery of a genetic mutation associated with Rett syndrome, research using gene therapy is underway. Stem cell therapy, alone or in combination with gene therapy, is another hopeful treatment that requires thorough study.

Abnormalities 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. Studies are underway to evaluate various treatments, such as busperidone (Buspar), naltraxone, or magnesium citrate.

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 daughter will grow accustomed to the abnormal breathing pattern.


Support Groups:

For additional information and resources, see the International Rett Syndrome Association.


Expectations (prognosis):

The progression of this disease usually levels off once the patient reaches teenage years. For example, if seizures or breathing abnormalities are present, they tend to lessen in late adolescence.

Each child's developmental regression or delays are different, so it is hard to generalize. Usually, a child with Rett syndrome sits up properly but may not crawl. For those who do crawl, many do so without using their hands (for example, "combat crawling" on the tummy).

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