Literature DB >> 17405857

Severe receptive language disorder in childhood--familial aspects and long-term outcomes: results from a Scottish study.

Ann Clark1, Anne O'Hare, Jocelynne Watson, Wendy Cohen, Hilary Cowie, Rob Elton, Jamal Nasir, Jonathan Seckl.   

Abstract

BACKGROUND AND AIMS: Little is known about the familial characteristics of children with severe receptive specific language impairment (SLI). Affected children are more likely to have long-term problems than those with expressive SLI but to date they have only been described as small cohorts within SLI populations. We therefore aimed to describe the clinical and familial characteristics of severe receptive SLI as defined by a rigorous phenotype and to establish whether non-word repetition showed a relationship with language impairment in these families.
METHODS: Cross-sectional study of children who met ICD-10 (F80.2) criteria for receptive SLI at school entry, their siblings and genetic parents with standardised measures of language and non-verbal IQ, phonological auditory memory and speech sound inventory.
RESULTS: At a mean of 6 years after school entry with a severe receptive SLI, the 58 participants had a normal mean and standard deviation non-verbal IQ, but only 3% (two) had attained language measures in the normal range. One third still had severe receptive language impairment. One third of siblings not known to be affected had language levels outside the normal range. Phonological auditory memory was impaired in most family members.
CONCLUSION: Severe receptive SLI is nearly always associated with an equally severe reduction in expressive language skills. Language impairment in siblings may go undetected and yet they are at high risk. Family members had weak phonological auditory memory skills, suggesting that this could be a marker for language acquisition difficulties. Receptive SLI rarely resolves and trials of therapy are urgently needed.

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Year:  2007        PMID: 17405857      PMCID: PMC2083799          DOI: 10.1136/adc.2006.101758

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  34 in total

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2.  Family genetic studies.

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  9 in total

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3.  Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Authors:  D F Newbury; S Paracchini; T S Scerri; L Winchester; L Addis; Alex J Richardson; J Walter; J F Stein; J B Talcott; A P Monaco
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Authors:  Pía Villanueva; Ron Nudel; Alexander Hoischen; María Angélica Fernández; Nuala H Simpson; Christian Gilissen; Rose H Reader; Lillian Jara; María Magdalena Echeverry; Maria Magdalena Echeverry; Clyde Francks; Gillian Baird; Gina Conti-Ramsden; Anne O'Hare; Patrick F Bolton; Elizabeth R Hennessy; Hernán Palomino; Luis Carvajal-Carmona; Joris A Veltman; Jean-Baptiste Cazier; Zulema De Barbieri; Simon E Fisher; Dianne F Newbury
Journal:  PLoS Genet       Date:  2015-03-17       Impact factor: 5.917

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7.  Qualitative aspects of developmental language impairment relate to language and literacy outcome in adulthood.

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8.  The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.

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9.  CMIP and ATP2C2 modulate phonological short-term memory in language impairment.

Authors:  Dianne F Newbury; Laura Winchester; Laura Addis; Silvia Paracchini; Lyn-Louise Buckingham; Ann Clark; Wendy Cohen; Hilary Cowie; Katharina Dworzynski; Andrea Everitt; Ian M Goodyer; Elizabeth Hennessy; A David Kindley; Laura L Miller; Jamal Nasir; Anne O'Hare; Duncan Shaw; Zoe Simkin; Emily Simonoff; Vicky Slonims; Jocelynne Watson; Jiannis Ragoussis; Simon E Fisher; Jonathon R Seckl; Peter J Helms; Patrick F Bolton; Andrew Pickles; Gina Conti-Ramsden; Gillian Baird; Dorothy V M Bishop; Anthony P Monaco
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  9 in total

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