Journal article
Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome
A Brignell, C Gu, A Holm, B Carrigg, DA Sheppard, DJ Amor, AT Morgan
European Journal of Human Genetics | SPRINGERNATURE | Published : 2021
Abstract
Communication difficulties are a core feature of Phelan-McDermid syndrome (PMS). However, a specific speech and language phenotype has not been delineated, preventing prognostic counselling and development of targeted therapies. We examined speech, language, social and functional communication abilities in 21 individuals with PMS (with SHANK3 involvement), using standardised assessments. Mean age was 9.7 years (SD 4.1) and 57% were female. Deletion size ranged from 41 kb to 8.3 Mb. Nine participants (45%) were non-verbal. Four (19%) had greater verbal ability, speaking in at least 4–5 word sentences, but with speech sound errors. Standard scores for receptive and expressive language were low..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
Funding was provided by National Health and Medical Research Council (NHMRC) Practitioner Fellowship #1105008 (A.M.); NHMRC Centre of Research Excellence in Speech and Language Neurobiology #1116976 awarded to A.M., D.A.