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Article

Characterization of speech and language phenotype in the 8p23.1 syndrome.

European child & adolescent psychiatry - 1 Oct 2024

Karsan Çağdaş, Ocak Feyzanur, Bulut Talat

Abstract excerpt

The 8p23.1 duplication syndrome is a rare genetic condition with an estimated prevalence rate of 1 out of 58,000. Although the syndrome was associated with speech and language delays, a comprehensive assessment of speech and language functions has not been undertaken in this population. To address this issue, the present study reports rigorous speech and language, in addition to oral-facial and developmental,...

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Identifiers

PMID: 38671247
DOI: 10.1007/s00787-024-02448-0
PMCID: PMC11564291

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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