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Article

Genotype and early development in Rett syndrome: the value of international data.

Brain & development - 1 Nov 2005

Leonard Helen, Moore Hannah, Carey Mary, Fyfe Susan, Hall Sonj, Robertson Laila, Wu Xi Ru, Bao Xinhua, Pan Hong, Christodoulou John, Williamson Sarah, Klerk Nick de

Abstract excerpt

BACKGROUND: Rett syndrome is a neurodevelopmental disorder mostly affecting females and caused by mutations in the MECP2 gene. Originally the syndrome was characterised as having a normal prenatal and perinatal period with later regression. Previous work has speculated that the girl with Rett syndrome may not be normal at birth. AIMS: to examine whether early development between birth and ten months varies by...

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Source

Identifiers

PMID: 16182492
DOI: 10.1016/j.braindev.2005.03.023

Genes

MECP2

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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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