Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35062
Title: Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.
Austin Authors: Morison, Lottie D;Kennis, Milou G P;Rots, Dmitrijs;Bouman, Arianne;Kummeling, Joost;Palmer, Elizabeth;Vogel, Adam P;Liegeois, Frederique;Brignell, Amanda;Srivastava, Siddharth;Frazier, Zoe;Milnes, Di;Goel, Himanshu;Amor, David J;Scheffer, Ingrid E ;Kleefstra, Tjitske;Morgan, Angela T
Affiliation: Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.;Department of Audiology and Speech Pathology, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Clinical Genetics, Radboudumc, Nijmegen, Netherlands.
Sydney Children's Hospital Network, Randwick, New South Wales, Australia.;Discipline of Paediatrics and Child Health, Faculty of Medicine and Health, University of New South Wales, Sydney, New South Wales, Australia.
Department of Audiology and Speech Pathology, The University of Melbourne, Melbourne, Victoria, Australia.;Redenlab, Melbourne, Victoria, Australia.
Great Ormond Street Institute of Child Health, University College London, London, UK.
Department of Paediatrics, Monash University, Clayton, Victoria, Australia.;Department of Developmental Paediatrics, Monash Children's Hospital, Clayton, Victoria, Australia.
Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Genetic Health Queensland, Herston, Queensland, Australia.
Hunter Genetics, Waratah, New South Wales, Australia.
Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.;Department of Paediatrics, Royal Children's Hospital, Parkville, Victoria, Australia.
Melbourne Brain Centre, Austin Health, Heidelberg, Victoria, Australia.
Department of Clinical Genetics, Radboudumc, Nijmegen, Netherlands.;Department of Clinical Genetics, Erasmus MC, Rotterdam, Netherlands.
Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.;Department of Audiology and Speech Pathology, The University of Melbourne, Melbourne, Victoria, Australia.
The Florey Institute of Neuroscience and Mental Health
Issue Date: 30-Jan-2024
Date: 2024
Publication information: Journal of Medical Genetics 2024-01-30
Abstract: Speech and language impairments are core features of the neurodevelopmental genetic condition Kleefstra syndrome. Communication has not been systematically examined to guide intervention recommendations. We define the speech, language and cognitive phenotypic spectrum in a large cohort of individuals with Kleefstra syndrome. 103 individuals with Kleefstra syndrome (40 males, median age 9.5 years, range 1-43 years) with pathogenic variants (52 9q34.3 deletions, 50 intragenic variants, 1 balanced translocation) were included. Speech, language and non-verbal communication were assessed. Cognitive, health and neurodevelopmental data were obtained. The cognitive spectrum ranged from average intelligence (12/79, 15%) to severe intellectual disability (12/79, 15%). Language ability also ranged from average intelligence (10/90, 11%) to severe intellectual disability (53/90, 59%). Speech disorders occurred in 48/49 (98%) verbal individuals and even occurred alongside average language and cognition. Developmental regression occurred in 11/80 (14%) individuals across motor, language and psychosocial domains. Communication aids, such as sign and speech-generating devices, were crucial for 61/103 (59%) individuals including those who were minimally verbal, had a speech disorder or following regression. The speech, language and cognitive profile of Kleefstra syndrome is broad, ranging from severe impairment to average ability. Genotype and age do not explain the phenotypic variability. Early access to communication aids may improve communication and quality of life.
URI: https://ahro.austin.org.au/austinjspui/handle/1/35062
DOI: 10.1136/jmg-2023-109702
ORCID: 0000-0003-2822-6522
0000-0002-3505-2631
0000-0001-7008-1879
0000-0003-1147-7405
Journal: Journal of Medical Genetics
PubMed URL: 38290825
ISSN: 1468-6244
Type: Journal Article
Subjects: Genetics, Behavioral
Human Genetics
Neurology
Pediatrics
Phenotype
Appears in Collections:Journal articles

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