In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting

التفاصيل البيبلوغرافية
العنوان: In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting
المؤلفون: Lottie D, Morison, Elisabeth, Meffert, Miriam, Stampfer, Irene, Steiner-Wilke, Brigitte, Vollmer, Katrin, Schulze, Tracy, Briggs, Ruth, Braden, Adam, Vogel, Daisy, Thompson-Lake, Chirag, Patel, Edward, Blair, Himanshu, Goel, Samantha, Turner, Ute, Moog, Angelika, Riess, Frederique, Liegeois, David A, Koolen, David J, Amor, Tjitske, Kleefstra, Simon E, Fisher, Christiane, Zweier, Angela T, Morgan
المصدر: Journal of medical genetics.
سنة النشر: 2022
الوصف: Heterozygous disruptions ofHere we phenotyped 28 individuals from 17 families with pathogenicSpeech disorders were prevalent (23/25, 92%) and CAS was most common (22/25, 88%), with similar speech presentations across English and German. Speech was still impaired in adulthood, and some speech sounds (eg, 'th', 'r', 'ch', 'j') were never acquired. Language impairments (21/25, 84%) ranged from mild to severe. Comorbidities included feeding difficulties in infancy (10/27, 37%), fine (13/26, 50%) and gross (13/26, 50%) motor impairment, anxiety (5/27, 19%), depression (6/27, 22%) and sleep disturbance (11/15, 44%). Physical features were common (22/27, 81%) but with no consistent pattern. Cognition ranged from average to mildly impaired and was incongruent with language ability; for example, seven participants with severe language disorder had average non-verbal cognition.Although we identify an increased prevalence of conditions like anxiety, depression and sleep disturbance, we confirm that the consequences of
تدمد: 1468-6244
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::284d1af41e20cfb3a2680a70bcd5ba17
https://pubmed.ncbi.nlm.nih.gov/36328423
رقم الأكسشن: edsair.pmid..........284d1af41e20cfb3a2680a70bcd5ba17
قاعدة البيانات: OpenAIRE