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Article

Rett syndrome: an eye-tracking study of attention and recognition memory.

Developmental medicine and child neurology - 1 Apr 2013

Rose Susan A, Djukic Aleksandra, Jankowski Jeffery J, Feldman Judith F, Fishman Iris, Valicenti-McDermott Maria

Abstract excerpt

AIM: The aim of this study was to examine attention and recognition memory for faces and patterns in Rett syndrome, a severely disabling neurodevelopmental disorder caused by mutations in the X-linked MECP2 gene. METHOD: Because Rett syndrome impairs speech and hand use, precluding most neuropsychological testing, the visual paired-comparison paradigm (VPC) was used, together with eye tracking. In the VPC, two...

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Source

Identifiers

PMID: 23488948
DOI: 10.1111/dmcn.12085

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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