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[Rett syndrome: from pathophysiology to developments in treatment]
Ana M Cabal-Herrera1, Christopher W Beatty2
1Department of Pediatrics, Division of Neurology, Nationwide Children's Hospital - The Ohio State University, USA.
Medicina
|September 27, 2024
Summary
Rett Syndrome (RTT) is a rare neurodevelopmental disorder in females caused by MECP2 gene mutations. This article overviews RTT diagnosis, its natural progression, and current treatment strategies.
Area of Science:
- Neuroscience
- Genetics
- Pediatrics
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