TY - JOUR
T1 - Expanding the phenotype of Kleefstra syndrome
T2 - speech, language and cognition in 103 individuals
AU - Morison, Lottie D.
AU - Kennis, Milou G.P.
AU - Rots, Dmitrijs
AU - Bouman, Arianne
AU - Kummeling, Joost
AU - Palmer, Elizabeth
AU - Vogel, Adam P.
AU - Liegeois, Frederique
AU - Brignell, Amanda
AU - Srivastava, Siddharth
AU - Frazier, Zoe
AU - Milnes, Di
AU - Goel, Himanshu
AU - Amor, David J.
AU - Scheffer, Ingrid E.
AU - Kleefstra, Tjitske
AU - Morgan, Angela T.
N1 - Funding Information:
Funding was provided by the National Health and Medical Research Council (NHMRC) Practitioner Fellowship (1105008; ATM); NHMRC Investigator Grant (1195955; ATM); NHMRC Centre of Research Excellence Translational Centre for Speech Disorders (2015727; ATM); Dutch Research Council Grant (015.014.036 and 1160.18.320; TK); the Netherlands Organisation for Health Research and Development (91718310 and 10250022110003; TK); NHMRC Postgraduate Scholarship (2022156; LDM); Australian Research Council Future Fellowship (220100253; AV); and the National Institutes of Health/National Institutes of Neurological Disorders and Stroke (K23NS119666; SS). This work was supported by the Victorian Government\u2019s Operational Infrastructure Support Program.
Publisher Copyright:
© 2024 Author(s) (or their employer(s)).
PY - 2024/6
Y1 - 2024/6
N2 - Objectives 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. Method 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. Results 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. Conclusions 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.
AB - Objectives 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. Method 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. Results 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. Conclusions 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.
KW - Genetics Behavioral
KW - Human Genetics
KW - Neurology
KW - Pediatrics
KW - Phenotype
UR - http://www.scopus.com/inward/record.url?scp=85194111673&partnerID=8YFLogxK
U2 - 10.1136/jmg-2023-109702
DO - 10.1136/jmg-2023-109702
M3 - Article
C2 - 38290825
AN - SCOPUS:85194111673
SN - 0022-2593
VL - 61
SP - 578
EP - 585
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
IS - 6
ER -