Rett’s autism, more commonly known as Rett syndrome, is a rare neurological disorder that affects brain development. It primarily occurs in girls and is often noticed after a period of typical growth in early childhood. While it shares traits with autism, such as communication challenges and repetitive behaviors, it is considered a distinct condition.
Key Symptoms:
- Loss of speech and motor skills after early normal development
- Repetitive hand movements (like wringing or clapping)
- Breathing irregularities
- Seizures and developmental delays
Causes: Rett’s autism is usually linked to mutations in the MECP2 gene. Unlike autism spectrum disorder, it is not caused by a wide range of genetic or environmental factors.
Treatment: There is no cure, but therapies such as ABA, physical therapy, and speech therapy can greatly improve quality of life.
At Bluebell ABA, we provide specialized support to help children with Rett’s autism build communication, independence, and daily living skills.
Frequently Asked Questions
1. Is Rett’s autism the same as autism?
No, it is a separate neurological disorder with some overlapping traits.
2. Can boys have Rett’s autism?
Yes, but it is extremely rare and often more severe.
3. How early can Rett’s autism be detected?
Signs typically appear between 6 and 18 months of age.
Sources:
- https://www.rettsyndrome.org/about-rett-syndrome/understanding-rett-syndrome/
- https://pmc.ncbi.nlm.nih.gov/articles/PMC5798978/