Literature DB >> 20543023

The language phenotype of children and adolescents with Noonan syndrome.

Elizabeth I Pierpont1, Susan Ellis Weismer, Amy E Roberts, Erica Tworog-Dube, Mary Ella Pierpont, Nancy J Mendelsohn, Mark S Seidenberg.   

Abstract

PURPOSE: This study presents an analysis of language skills in individuals with Noonan syndrome (NS), an autosomal dominant genetic disorder. We investigated whether the language impairments affecting some individuals arise from deficits specifically within the linguistic system or whether they are associated with cognitive, perceptual, and motor factors. Comparisons of language abilities among the different NS genotypes were also conducted.
METHOD: Sixty-six children and adolescents with NS were evaluated using standardized speech, language, and literacy assessments. Additional cognitive, perceptual, and motor tasks were administered to examine the relation of these factors to language development. Genotype was noted for those who underwent genetic testing.
RESULTS: Language impairments were more frequent in NS than in the general population and were associated with higher risk for reading and spelling difficulties. Language was significantly correlated with nonverbal cognition, hearing ability, articulation, motor dexterity, and phonological memory. Genotype analyses suggest that the higher performance of SOS1-positive than PTPN11-positive individuals on language tasks was largely mediated by differences in cognitive ability.
CONCLUSIONS: Our results indicate that variation in language skill in NS is closely related to cognitive, perceptual, and motor factors. It does not appear that specific aspects of language are selectively affected in this syndrome.

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Year:  2010        PMID: 20543023      PMCID: PMC3086511          DOI: 10.1044/1092-4388(2009/09-0046)

Source DB:  PubMed          Journal:  J Speech Lang Hear Res        ISSN: 1092-4388            Impact factor:   2.297


  64 in total

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2.  Clinical and molecular studies in a large Dutch family with Noonan syndrome.

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Journal:  Otolaryngol Head Neck Surg       Date:  1998-03       Impact factor: 5.591

6.  Clinical decision making: describing the decision rules of practicing speech-language pathologists.

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Journal:  J Speech Hear Res       Date:  1994-02

7.  Lexical representations in children with SLI: evidence from a frequency-manipulated gating task.

Authors:  Elina Mainela-Arnold; Julia L Evans; Jeffry A Coady
Journal:  J Speech Lang Hear Res       Date:  2008-04       Impact factor: 2.297

8.  A longitudinal investigation of reading outcomes in children with language impairments.

Authors:  Hugh W Catts; Marc E Fey; J Bruce Tomblin; Xuyang Zhang
Journal:  J Speech Lang Hear Res       Date:  2002-12       Impact factor: 2.297

9.  Germline KRAS mutations cause Noonan syndrome.

Authors:  Suzanne Schubbert; Martin Zenker; Sara L Rowe; Silke Böll; Cornelia Klein; Gideon Bollag; Ineke van der Burgt; Luciana Musante; Vera Kalscheuer; Lars-Erik Wehner; Hoa Nguyen; Brian West; Kam Y J Zhang; Erik Sistermans; Anita Rauch; Charlotte M Niemeyer; Kevin Shannon; Christian P Kratz
Journal:  Nat Genet       Date:  2006-02-12       Impact factor: 38.330

10.  Are specific language impairment and dyslexia distinct disorders?

Authors:  Hugh W Catts; Suzanne M Adlof; Tiffany P Hogan; Susan Ellis Weismer
Journal:  J Speech Lang Hear Res       Date:  2005-12       Impact factor: 2.297

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  8 in total

1.  Effects of germline mutations in the Ras/MAPK signaling pathway on adaptive behavior: cardiofaciocutaneous syndrome and Noonan syndrome.

Authors:  Elizabeth I Pierpont; Mary Ella Pierpont; Nancy J Mendelsohn; Amy E Roberts; Erica Tworog-Dube; Katherine A Rauen; Mark S Seidenberg
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

Review 2.  Genetic insights into the functional elements of language.

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3.  Intellectual development in Noonan syndrome: a longitudinal study.

Authors:  Renée L Roelofs; Nikki Janssen; Ellen Wingbermühle; Roy P C Kessels; Jos I M Egger
Journal:  Brain Behav       Date:  2016-05-03       Impact factor: 2.708

4.  Social skills in children with RASopathies: a comparison of Noonan syndrome and neurofibromatosis type 1.

Authors:  Elizabeth I Pierpont; Rebekah L Hudock; Allison M Foy; Margaret Semrud-Clikeman; Mary Ella Pierpont; Susan A Berry; Ryan Shanley; Nathan Rubin; Katherine Sommer; Christopher L Moertel
Journal:  J Neurodev Disord       Date:  2018-06-18       Impact factor: 4.025

5.  The Noonan Syndrome-linked Raf1L613V mutation drives increased glial number in the mouse cortex and enhanced learning.

Authors:  Michael C Holter; Lauren T Hewitt; Stephanie V Koebele; Jessica M Judd; Lei Xing; Heather A Bimonte-Nelson; Cheryl D Conrad; Toshiyuki Araki; Benjamin G Neel; William D Snider; Jason M Newbern
Journal:  PLoS Genet       Date:  2019-04-24       Impact factor: 5.917

6.  Defining language disorders in children and adolescents with Noonan Syndrome.

Authors:  Giulia Lazzaro; Cristina Caciolo; Deny Menghini; Francesca Cumbo; Maria C Digilio; Rossella Capolino; Giuseppe Zampino; Marco Tartaglia; Stefano Vicari; Paolo Alfieri
Journal:  Mol Genet Genomic Med       Date:  2020-02-14       Impact factor: 2.183

Review 7.  Noonan syndrome.

Authors:  Amy E Roberts; Judith E Allanson; Marco Tartaglia; Bruce D Gelb
Journal:  Lancet       Date:  2013-01-10       Impact factor: 79.321

8.  Pragmatic language impairment in children with Noonan syndrome.

Authors:  Magnhild Selås; Wenche Andersen Helland
Journal:  Clin Linguist Phon       Date:  2016-06-27       Impact factor: 1.346

  8 in total

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