Health condition · plain-language reference
Rett Syndrome
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
Plain-language summary from MedlinePlus (NIH/NLM) ↗. For informational purposes only — not medical advice.
Medications used for rett syndrome
Drugs whose FDA labeling names this condition among its indications — informational, not a recommendation.
- HaloperidolTypical Antipsychotic [EPC]›
- RisperidoneAtypical Antipsychotic [EPC]›
- AripiprazoleAtypical Antipsychotic [EPC]›
- TrofinetideCytochrome P450 3A4 Inhibitors [MoA]›
- Aripiprazole OralAtypical Antipsychotic [EPC]›
- Aripiprazole Orally DisintegratingAtypical Antipsychotic [EPC]›
- PimozideTypical Antipsychotic [EPC]›
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