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Article

Health service use in Rett syndrome.

Journal of child neurology - 1 Jan 2005

Moore Hannah, Leonard Helen, de Klerk Nick, Robertson Ian, Fyfe Sue, Christodoulou John, Weaving Linda, Davis Mark, Mulroy Seonaid, Colvin Lyn

Abstract excerpt

Rett syndrome is a severe neurodevelopmental disorder affecting girls, caused by mutations in the MECP2 gene. There are no population-based data on the extent and determinants of health service use in this disorder. The population-based registry, the Australian Rett Syndrome database, was the source of phenotype data. This also contains data from mutation screening and X-inactivation studies. Data on...

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Source

Identifiers

PMID: 15791922
DOI: 10.1177/08830738050200010701

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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