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Article

Global prevalence of Rett syndrome: systematic review and meta-analysis.

Systematic reviews - 16 Jan 2023

Petriti Uarda, Dudman Daniel C, Scosyrev Emil, Lopez-Leon Sandra

Abstract excerpt

BACKGROUND: Rett syndrome is a rare, severe neurodevelopmental disorder. Almost all cases occur in girls, in association with spontaneous (non-inherited) mutations involving the methyl-CpG-binding protein 2 gene located on the X chromosome. Diagnostic criteria for typical Rett syndrome require a period of regression, followed by recovery or stabilization, and fulfillment of all four main criteria (loss of...

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Identifiers

PMID: 36642718
DOI: 10.1186/s13643-023-02169-6
PMCID: PMC9841621

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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