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Article

Severe speech impairment is a distinguishing feature of FOXP1-related disorder.

Developmental medicine and child neurology - 1 Dec 2021

Braden Ruth O, Amor David J, Fisher Simon E, Mei Cristina, Myers Candace T, Mefford Heather, Gill Deepak, Srivastava Siddharth, Swanson Lindsay C, Goel Himanshu, Scheffer Ingrid E, Morgan Angela T

Abstract excerpt

AIM: To delineate the speech and language phenotype of a cohort of individuals with FOXP1-related disorder. METHOD: We administered a standardized test battery to examine speech and oral motor function, receptive and expressive language, non-verbal cognition, and adaptive behaviour. Clinical history and cognitive assessments were analysed together with speech and language findings. RESULTS: Twenty-nine patients...

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Source

Identifiers

PMID: 34109629
DOI: 10.1111/dmcn.14955

Genes

FOXP1

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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