Speech in children with cerebral palsy

Journal article


Mei, Cristina, Reilly, Sheena, Bickerton, Molly, Mensah, Fiona, Turner, Samantha, Kumaranayagam, Dhanooshini, Pennington, Lindsay, Reddihough, Dinah and Morgan, Angela T.. (2020). Speech in children with cerebral palsy. Developmental Medicine and Child Neurology. 62(12), pp. 1374-1382. https://doi.org/10.1111/dmcn.14592
AuthorsMei, Cristina, Reilly, Sheena, Bickerton, Molly, Mensah, Fiona, Turner, Samantha, Kumaranayagam, Dhanooshini, Pennington, Lindsay, Reddihough, Dinah and Morgan, Angela T.
Abstract

Aim
To examine the frequency, characteristics, and factors associated with speech delay and disorder in a community sample of children with cerebral palsy (CP).

Method
Participants were 84 children (37 females, 47 males; aged between 4y 11mo–6y 6mo) with CP identified through a population-based registry. Speech and oromotor function were systematically evaluated to provide a differential diagnosis of articulation, phonological, and motor speech disorders.

Results
In total, 82% (69/84) of participants had delayed or disordered speech production, including minimally verbal presentations (n=20). Verbal participants (n=64) presented with dysarthria (78%), articulation delay or disorder (54%), phonological delay or disorder (43%), features of childhood apraxia of speech (CAS) (17%), or mixed presentations across these conditions. Speech intelligibility was poorest in those with dysarthria and features of CAS. Speech delay or disorder in verbal participants was associated with language impairment (p=0.002) and reduced health-related quality of life (p=0.04) (Fisher’s exact test). Poorer speech accuracy (i.e. lower percentage consonants correct) correlated with greater impairments in both language (p<0.001) and oromotor function (p<0.001) (Spearman’s test).

Interpretation
The speech profile of children with CP is characterized by impairment at multiple levels of speech production (phonetic, cognitive-linguistic, neuromuscular execution, and high-level planning/programming), highlighting the importance of a personalized differential diagnosis informing targeted treatment.

Year2020
JournalDevelopmental Medicine and Child Neurology
Journal citation62 (12), pp. 1374-1382
PublisherBlackwell Publishing Ltd
ISSN0012-1622
Digital Object Identifier (DOI)https://doi.org/10.1111/dmcn.14592
Scopus EID2-s2.0-85087176166
Research or scholarlyResearch
Page range1374-1382
FunderNational Health and Medical Research Council (NHMRC)
Publisher's version
License
All rights reserved
File Access Level
Controlled
Output statusPublished
Publication dates
Online26 Jun 2020
Publication process dates
Accepted29 Apr 2020
Deposited20 Aug 2021
Grant IDNHMRC/607448
NHMRC/607314
NHMRC/1105008
NHMRC/491210
NHMRC/1041892
NHMRC/1037449
NHMRC/1111160
Permalink -

https://acuresearchbank.acu.edu.au/item/8w9z0/speech-in-children-with-cerebral-palsy

Restricted files

Publisher's version

  • 65
    total views
  • 0
    total downloads
  • 0
    views this month
  • 0
    downloads this month
These values are for the period from 19th October 2020, when this repository was created.

Export as

Related outputs

Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
Morgan, Angela, Scerri, T.S., Vogel, Adam P., Reid, Christopher A., Quach, Mara, Jackson, Victoria, McKenzie, Chaseley, Burrows, Emma L., Bennett, Mark F., Turner, Samantha, Reilly, Sheena, Horton, Sarah E., Block, Susan, Kefalianos, Elaina, Frigerio-Domingues, Carlos and et. al.. (2023). Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain. 146(12), pp. 5086-5097. https://doi.org/10.1093/brain/awad314
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2
Morison, Lottie D., Meffert, Elisabeth, Stampfer, Miriam, Steiner-Wilke, Irene, Vollmer, Brigitte, Schulze, Katrin, Briggs, Tracy, Braden, Ruth, Vogel, Adam, Thompson-Lake, Daisy G. Y, Patel, Chirag, Blair, Edward, Goel, Himanshu, Turner, Samantha, Moog, Ute, Riess, Angelika, Liegeois, Frederique, Koolen, David A, Amor, David J., ... Morgan, Angela T.. (2023). In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. Journal of Medical Genetics. 60(6), pp. 597-607. https://doi.org/10.1136/jmg-2022-108734
Atypical development of Broca's area in a large family with inherited stuttering
Thompson-Lake, Daisy G. Y, Scerri, Thomas S., Block, Susan, Turner, Samantha J., Reilly, Sheena, Kefalianos, Elaina, Bonthrone, Alexandra F., Helbig, Ingo, Bahlo, Melanie, Scheffer, Ingrid E., Hildebrand, Michael S., Liégeois, Frédérique J. and Morgan, Angela T.. (2022). Atypical development of Broca's area in a large family with inherited stuttering. Brain. 145(3), pp. 1177-1188. https://doi.org/10.1093/brain/awab364
Severe childhood speech disorder : Gene discovery highlights transcriptional dysregulation
Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Van Reyk, Olivia, Coleman, Matthew, Braden, Ruth O., Turner, Samantha, Rigbye, Kristin A., Boys, Amber, Barton, Sarah, Webster, Richard, Fahey, Michael, Saunders, Kerryn, Parry-Fielder, Bronwyn, Paxton, Georgia, Hayman, Michael, Coman, David, Goel, Himanshu, Baxter, Anne, ... Morgan, Angela T.. (2020). Severe childhood speech disorder : Gene discovery highlights transcriptional dysregulation. Neurology. 94(20), pp. e2148-e2167. https://doi.org/10.1212/WNL.0000000000009441
Looking to the future : Speech, language, and academic outcomes in an adolescent with childhood apraxia of speech
Turner, Samantha J., Vogel, Adam P., Parry-Fielder, Bronwyn, Campbell, Rhonda, Scheffer, Ingrid E. and Morgan, Angela T.. (2019). Looking to the future : Speech, language, and academic outcomes in an adolescent with childhood apraxia of speech. Folia Phoniatrica et Logopaedica. 71(5-6), pp. 203-215. https://doi.org/10.1159/000500554
Dorsal language stream anomalies in an inherited speech disorder
Liégeois, Frédérique J., Turner, Samantha J., Mayes, Angela, Bonthrone, Alexandra F., Boys, Amber, Smith, Libby, Parry-Fielder, Bronwyn, Mandelstam, Simone, Spencer-Smith, Megan, Bahlo, Melanie, Scerri, Tom S., Hildebrand, Michael S., Scheffer, Ingrid E., Connelly, Alan and Morgan, Angela T.. (2019). Dorsal language stream anomalies in an inherited speech disorder. Brain: a journal of neurology. 142(4), pp. 966-977. https://doi.org/10.1093/brain/awz018
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations
Corbett, Mark A., Turner, Samantha J., Gardner, Alison, Silver, Jeremy, Stankovich, Jim, Leventer, Richard J., Derry, Christopher P., Carroll, Renee, Ha, Thuong, Scheffer, Ingrid E., Bahlo, Melanie, Jackson, Graeme D., Mackey, David A., Berkovic, Samuel F. and Gecz, Jozef. (2017). Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. European Journal of Medical Genetics. 60(8), pp. 437-443. https://doi.org/10.1016/j.ejmg.2017.06.002
Dysarthria and broader motor speech deficits in Dravet syndrome
Turner, Samantha J., Brown, Amy, Arpone, Marta, Anderson, Vicki, Morgan, Angela T. and Scheffer, Ingrid E.. (2017). Dysarthria and broader motor speech deficits in Dravet syndrome. Neurology. 88(8), pp. 743-749. https://doi.org/10.1212/WNL.0000000000003635
Early neuroimaging markers of FOXP2 intragenic deletion
Liégeois, Frédérique J., Hildebrand, Michael S., Bonthrone, Alexandra, Turner, Samantha J., Scheffer, Ingrid E., Bahlo, Melanie, Connelly, Alan and Morgan, Angela T.. (2016). Early neuroimaging markers of FOXP2 intragenic deletion. Scientific Reports. 6, p. Article: 35192. https://doi.org/10.1038/srep35192
GRIN2A : An aptly named gene for speech dysfunction
Turner, Samantha, Mayes, Angela K., Verhoeven, Andrea, Mandelstam, Simone A., Morgan, Angela and Scheffer, Ingrid E.. (2015). GRIN2A : An aptly named gene for speech dysfunction. Neurology. 84(6), pp. 586-593. https://doi.org/10.1212/WNL.0000000000001228