Back to Search Start Over

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

Authors :
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
Source :
Developmental Medicine & Child Neurology; Dec2021, Vol. 63 Issue 12, p1417-1426, 10p
Publication Year :
2021

Abstract

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 (17 females, 12 males; mean age 9y 6mo; median age 8y [range 2y 7mo–33y]; SD 6y 5mo) with pathogenic FOXP1 variants (14 truncating, three missense, three splice site, one in‐frame deletion, eight cytogenic deletions; 28 out of 29 were de novo variants) were studied. All had atypical speech, with 21 being verbal and eight minimally verbal. All verbal patients had dysarthric and apraxic features, with phonological deficits in most (14 out of 16). Language scores were low overall. In the 21 individuals who carried truncating or splice site variants and small deletions, expressive abilities were relatively preserved compared with comprehension. Interpretation: FOXP1‐related disorder is characterized by a complex speech and language phenotype with prominent dysarthria, broader motor planning and programming deficits, and linguistic‐based phonological errors. Diagnosis of the speech phenotype associated with FOXP1‐related dysfunction will inform early targeted therapy. What this paper addsIndividuals with FOXP1‐related disorder have a complex speech and language phenotype.Dysarthria, which impairs intelligibility, is the dominant feature of the speech profile.No participants were receiving speech therapy for dysarthria, but were good candidates for therapyFeatures of speech apraxia occur alongside persistent phonological errors.Language abilities are low overall; however, expressive language is a relative strength. What this paper adds: Individuals with FOXP1‐related disorder have a complex speech and language phenotype.Dysarthria, which impairs intelligibility, is the dominant feature of the speech profile.No participants were receiving speech therapy for dysarthria, but were good candidates for therapyFeatures of speech apraxia occur alongside persistent phonological errors.Language abilities are low overall; however, expressive language is a relative strength. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00121622
Volume :
63
Issue :
12
Database :
Complementary Index
Journal :
Developmental Medicine & Child Neurology
Publication Type :
Academic Journal
Accession number :
153606136
Full Text :
https://doi.org/10.1111/dmcn.14955