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Article

Subclinical inflammatory status in Rett syndrome.

Mediators of inflammation - 1 Jan 2014

Cortelazzo Alessio, De Felice Claudio, Guerranti Roberto, Signorini Cinzia, Leoncini Silvia, Pecorelli Alessandra, Zollo Gloria, Landi Claudia, Valacchi Giuseppe, Ciccoli Lucia, Bini Luca, Hayek Joussef

Abstract excerpt

Inflammation has been advocated as a possible common central mechanism for developmental cognitive impairment. Rett syndrome (RTT) is a devastating neurodevelopmental disorder, mainly caused by de novo loss-of-function mutations in the gene encoding MeCP2. Here, we investigated plasma acute phase response (APR) in stage II (i.e., "pseudo-autistic") RTT patients by routine haematology/clinical chemistry and...

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Source

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Identifiers

PMID: 24511209
DOI: 10.1155/2014/480980
PMCID: PMC3913335

Genes

MECP2

Variants

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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