Publication date: Available online 5 June 2018
Source:Journal of Communication Disorders
Author(s): Ellen Van Den Heuvel, Eric Manders, Ann Swillen, Inge Zink
Background22q11.2 deletion syndrome (22q11.2DS) is a genetic condition associated with a highly variable phenotypic expression. During childhood speech and language deficits are commonly observed. Findings of cross-sectional studies suggest syndrome-specific and changing language profiles, but a longitudinal approach to identify developmental changes is still lacking to date.AimsThe present study aimed to delineate language characteristics and trajectories by comparing the performance of Dutch-speaking school-aged children with 22q11.2DS (n = 18) to those of peers with idiopathic intellectual disability (IID, n = 19) and to those of children with IID and comorbid autism spectrum disorder (IID + ASD, n = 23). The literature shows contradictory findings regarding language comprehension difficulties in children with 22q11.2DS, we focused on the receptive-expressive language discrepancy. Given their relative strength for verbal short-term memory (VSTM) tasks, a fine-grained error categorization was included to elucidate a possible influence of VSTM on the expressive language outcomes. Finally, we suggested that the inability of children with 22q11.2DS to use contextual information could interfere with morphosyntactic measures.MethodsAll groups (22q11.2DS, IID, and IID + ASD) were matched for nonverbal fluid reasoning (Gf) using the Analogies and Categories subtests of the Snijders-Oomen Nonverbal Intelligence Test or the Matrix Reasoning and Picture Concepts subtests of the Wechsler Preschool and Primary Scale of Intelligence. Several structural language skills were measured using the Clinical Evaluation of Language Fundamentals and Peabody Picture Vocabulary Test. The same instruments were re-administered after 18 to 24 months. A fine-grained error analysis of the Formulating and Recalling Sentences subtests, both measuring expressive syntax, explored factors contributing to expressive language deficits.ResultsIn children with 22q11.2DS the relative advantage of receptive over expressive language had decreased compared to children with IID. For children with 22q11.2DS, complex sentence comprehension remained very challenging over time. Expressive language skills seemed less limited compared to children with IID, and were accompanied by less VSTM difficulties. In children with 22q11.2DS and children with IID + ASD, variable patterns of strengths and weaknesses were demonstrated, resulting in subtle differences between these groups. Error analyses indicated disregard of content-contextual cues and use of vague and elliptic language as being typical for children with 22q11.2DS.ConclusionsWe recommend that in children with 22q11.2DS the impact of the receptive language impairment should be comprehensively examined and followed-up since it can have a negative effect on their social communication skills, adaptive functioning and academic achievement. Error analysis underscores that multiple measures should be used to evaluate the child's expressive language ability. Further research should focus on developmental trajectories of social communication skills and on the use of intervention strategies focusing on language comprehension and pragmatics in children with 22q11.2DS.
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Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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! # Ola via Alexandros G.Sfakianakis on Inoreader
Η λίστα ιστολογίων μου
Τρίτη 5 Ιουνίου 2018
ATYPICAL LANGUAGE CHARACTERISTICS AND TRAJECTORIES IN CHILDREN WITH 22Q11.2 DELETION SYNDROME
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- Perioperative management of patients with cancer p...
- Retraction notice to "Graphene quantum dots decora...
- Editorial Board
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- Relationship between complications and long-term p...
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- Polydrug use patterns, risk behavior and unmet hea...
- Psychometric evaluation of the drinking refusal se...
- Watch the Clock, Not the Scale
- Visualizing Fatty Acid Flux
- Obesity Protects Cancer from Drugs Targeting Blood...
- OXPHOS Defects Due to mtDNA Mutations: Glutamine t...
- Viral Vectors for Studying Brain Mechanisms that C...
- Of Mice Not Men? Actions of Interleukin-6 on Gluco...
- Hallmarks of Brain Aging: Adaptive and Pathologica...
- Intermittent Fasting Confers Protection in CNS Aut...
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- 12,13-diHOME: An Exercise-Induced Lipokine that In...
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- Save the Date: Dr. Steven Zeitels to Speak at ORL ...
- Amber Luong, MD, PhD Recognized as Trailblazer
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- Molecular targets of celastrol in cancer: Recent t...
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- Longitudinal accrual of neocortical amyloid burden...
- Cover 2: Editorial Advisory Board
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- DNAJC12 mutation is rare in Chinese Han population...
- Association analyses of variants of SIPA1L2, MIR46...
- Genome-wide association identifies a novel locus f...
- Mutation screening of the TIA1 gene in Chinese pat...
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- Relationship between concentration of rare earth e...
- Effect of salinity stress on phenotypic plasticity...
- Could Less Be More in Febrile Neutropenia, Too?
- Pain, psychiatric comorbidities, and psychosocial ...
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- Consensus Guidelines on the Use of Intravenous Ket...
- Consensus Guidelines on the Use of Intravenous Ket...
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- Does evidence support the use of cat allergen immu...
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- Needleless connector drying time—how long does it ...
- Exploring the use of entertainment-education YouTu...
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- Efficacy and safety of a novel skin cleansing form...
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- Bowel morbidity following radiochemotherapy and im...
- Longitudinal studies of the 18 F-FDG kinetics afte...
- Risk associated with engineered nanomaterials: Dif...
- Repetitive transcranial magnetic stimulation of th...
- MAGIC: an open-source MATLAB toolbox for external ...
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