Childhood motor speech disorders: who to prioritise for genetic testing.

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Title: Childhood motor speech disorders: who to prioritise for genetic testing.
Authors: Van Niel H; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia., Lauretta M; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia.; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia., Baker E; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia.; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia., O'Donnell L; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia.; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia., Boulton C; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia.; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia., Brenchley C; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia.; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia., Coman D; Queensland Children's Hospital, South Brisbane, QLD, Australia.; University of Queensland, St. Lucia, Brisbane, QLD, Australia., Michellis E; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia., Goel H; Hunter Genetics, John Hunter Hospital, New Lambton Heights, Newcastle, NSW, Australia., Thompson G; Burnside Hospital, Toorak Gardens, Adelaide, SA, Australia., Webster R; Neurology Department, The Children's Hospital at Westmead, Westmead, NSW, Australia., Paxton G; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia.; Department of Paediatrics, The University of Melbourne, Melbourne, Australia., Stark Z; Victorian Clinical Genetics Service, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia., Scheffer IE; Department of Paediatrics, The University of Melbourne, Melbourne, Australia.; Epilepsy Research Centre, Austin Health, Heidelberg, Melbourne, VIC, Australia., Hildebrand MS; Department of Paediatrics, The University of Melbourne, Melbourne, Australia.; Epilepsy Research Centre, Austin Health, Heidelberg, Melbourne, VIC, Australia.; Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia., Amor DJ; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia.; Department of Paediatrics, The University of Melbourne, Melbourne, Australia.; Victorian Clinical Genetics Service, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia., Morgan AT; Speech and Language, Genomics Theme, Murdoch Children's Research Institute, Parkville, Melbourne, VIC, Australia. angela.morgan@mcri.edu.au.; Royal Children's Hospital, Parkville, Melbourne, VIC, Australia. angela.morgan@mcri.edu.au.; University of Queensland, St. Lucia, Brisbane, QLD, Australia. angela.morgan@mcri.edu.au.; Department of Audiology and Speech Pathology, The University of Melbourne, Melbourne, VIC, Australia. angela.morgan@mcri.edu.au.
Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 May; Vol. 34 (5), pp. 639-648. Date of Electronic Publication: 2026 Jan 13.
Publication Type: Journal Article
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1476-5438
DOI:10.1038/s41431-025-01993-9