Classic Rett Syndrome with Developmental Regression and Epilepsy in a Four-Year-Old Child: A Case Report
S. Gurulakshmy, S. Balabaskaran & K. Devimeenakshi · Asian Journal of Pediatric Research · 2026
Rett syndrome is a rare neurodevelopmental disorder that predominantly affects girls and is commonly associated with pathogenic variants in the methyl-CpG-binding protein 2 (MECP2) gene. It is characterised by apparently normal early development followed by developmental regressi...
Open access
Research Article
10.9734/ajpr/2026/v16i5546