Literature DB >> 17428527

Evaluation of narrative abilities in patients suffering from Duchenne Muscular Dystrophy.

A Marini1, M L Lorusso, M G D'Angelo, F Civati, A C Turconi, F Fabbro, N Bresolin.   

Abstract

The present work investigated cognitive, linguistic and narrative abilities in a group of children suffering from Duchenne Muscular Dystrophy, an allelic X-linked recessive disorder caused by mutations in the gene encoding dystrophin. The patients showed mildly reduced IQ with lower Verbal than Performance Intelligence Quotient and were mildly affected in visual attention and short-term memory processing. At the linguistic assessment, neither receptive (word comprehension) nor expressive (naming tasks and fluency) lexical abilities were impaired. However, their narratives were qualitatively inferior with respect to those produced by a group of typically developing children. Their speech samples were characterized by the presence of fewer verbs and complete sentences. It is suggested that the reduced production of complete sentences is due to a selective problem in verb argument structure generation. Since the lack of dystrophin is assumed to produce effects on the maturation of the cerebellum, whose involvement has been recently suggested in verb and syntactic processing, these findings may lend indirect support to the hypothesis of a cerebellar-cortical circuit specialized in verb and sentence production.

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Year:  2007        PMID: 17428527     DOI: 10.1016/j.bandl.2007.02.003

Source DB:  PubMed          Journal:  Brain Lang        ISSN: 0093-934X            Impact factor:   2.381


  6 in total

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2.  Abnormalities in brain structure and biochemistry associated with mdx mice measured by in vivo MRI and high resolution localized (1)H MRS.

Authors:  Su Xu; Da Shi; Stephen J P Pratt; Wenjun Zhu; Andrew Marshall; Richard M Lovering
Journal:  Neuromuscul Disord       Date:  2015-07-10       Impact factor: 4.296

3.  Mechanisms and Consequences of Cerebellar Purkinje Cell Disinhibition in a Mouse Model of Duchenne Muscular Dystrophy.

Authors:  Wan-Chen Wu; Samual P Bradley; Jason M Christie; Jason R Pugh
Journal:  J Neurosci       Date:  2022-01-21       Impact factor: 6.709

4.  Cerebellar-dependent associative learning is preserved in Duchenne muscular dystrophy: a study using delay eyeblink conditioning.

Authors:  Ulrike Schara; Melanie Busse; Dagmar Timmann; Marcus Gerwig
Journal:  PLoS One       Date:  2015-05-14       Impact factor: 3.240

Review 5.  Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta.

Authors:  Maman Joyce Dogba; Frank Rauch; Erin Douglas; Christophe Bedos
Journal:  Health Qual Life Outcomes       Date:  2014-10-25       Impact factor: 3.186

Review 6.  Cognitive Deficits in Myopathies.

Authors:  Eleni Peristeri; Athina-Maria Aloizou; Paraskevi Keramida; Zisis Tsouris; Vasileios Siokas; Alexios-Fotios A Mentis; Efthimios Dardiotis
Journal:  Int J Mol Sci       Date:  2020-05-27       Impact factor: 5.923

  6 in total

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