Literature DB >> 20561146

Core neuropsychological characteristics of children and adolescents with 22q11.2 deletion.

C Jacobson1, J Shearer, A Habel, F Kane, E Tsakanikos, E Kravariti.   

Abstract

BACKGROUND: The 22q11.2 deletion syndrome (22qDS) confers high risk for intellectual disability and neuropsychological/academic impairment, although a minority of patients show average intelligence. Intellectual heterogeneity and the high prevalence of psychiatric diagnoses in earlier studies may have obscured the prototypical neuropsychological profile in 22qDS.
METHODS: We examined intelligence, memory, reading and mathematical processes in 31 children/adolescents with 22qDS, selected for educational underachievement and an absence of psychiatric diagnoses, using standardised, psychometrically matched instruments that specify how typical a score is for a given intelligence quotient (IQ).
RESULTS: Corroborating earlier findings, verbal IQ was significantly superior to performance IQ; verbal memory and basic reading were relative strengths; and visual/spatial memory was a relative weakness. All four findings transcended performance characteristics that are typical of low-IQ individuals. Rote learning yielded the highest score; reading comprehension, numerical operations and mathematical reasoning were among the lowest-performed academic domains. Albeit in the expected direction, performance in the respective components could not be clearly differentiated from what is IQ-appropriate.
CONCLUSIONS: A superiority of verbal intelligence over non-verbal intelligence, relative strengths in verbal memory and basic reading, and a relative weakness in visual/spatial memory are likely to be core characteristics of children/adolescents with 22qDS, transcending performance features that are typical of individuals with low IQ.

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Mesh:

Year:  2010        PMID: 20561146     DOI: 10.1111/j.1365-2788.2010.01298.x

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  13 in total

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Review 2.  Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.

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Journal:  Behav Genet       Date:  2011-05-15       Impact factor: 2.805

3.  Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.

Authors:  Ling M Wong; Tracy Riggins; Danielle Harvey; Margarita Cabaral; Tony J Simon
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Review 4.  22q11.2 deletion syndrome.

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5.  A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.

Authors:  Stephen R Hooper; Kathleen Curtiss; Kelly Schoch; Matcheri S Keshavan; Andrew Allen; Vandana Shashi
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6.  Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.

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7.  Functional outcomes of adults with 22q11.2 deletion syndrome.

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Review 8.  A cross-comparison of cognitive ability across 8 genomic disorders.

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9.  From Learning to Memory: A Comparison Between Verbal and Non-verbal Skills in 22q11.2 Deletion Syndrome.

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