Literature DB >> 22385039

Specific profiles of neurocognitive and reading functions in a sample of 42 Italian boys with Duchenne Muscular Dystrophy.

Maria Luisa Lorusso1, Federica Civati, Massimo Molteni, Anna Carla Turconi, Nereo Bresolin, Maria Grazia D'Angelo.   

Abstract

A group of 42 Italian boys with Duchenne Muscular Dystrophy was compared with a control group of 10 boys with Spinal Muscular Atrophy and Osteogenesis Imperfecta on tests assessing general intellectual ability, language, neuropsychological functions, and reading skills with the aim of describing a comprehensive profile of the various functions and investigating their interrelationships. The influence of general intellectual level on performance was analyzed. Further, correlations between various neuropsychological measures and language performances were computed for the group with Duchenne Muscular Dystrophy, as well as the correlations between reading scores and other cognitive and linguistic measures. A general lowering in VIQ, PIQ, and FSIQ scores was found to characterize the group with Duchenne Muscular Dystrophy. Expressive language skills were within the normal range, while syntactic and grammatical comprehension were significantly impaired. The presence of below-average reading performances was further confirmed. However, unlike previous studies on irregular orthographies, the present results show that (a) the mild reading difficulties found in the sample essentially concern speed rather than accuracy; (b) they concern word rather than nonword reading; (c) lower reading performances are related to lower scores in general IQ; (d) no correlations emerge with phonological abilities, verbal short-term memory, or working memory, but rather with long-term memory and lexical skills. This may suggest that language-specific effects modulate the cognitive expressions of Duchenne Muscular Dystrophy and raises the possibility that the dysfunctions underlying the reading difficulties observed in affected readers of regular orthographies involve different neurocognitive systems than the cortico-cerebellar circuits usually invoked.

Entities:  

Mesh:

Year:  2012        PMID: 22385039     DOI: 10.1080/09297049.2012.660912

Source DB:  PubMed          Journal:  Child Neuropsychol        ISSN: 0929-7049            Impact factor:   2.500


  5 in total

1.  Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system.

Authors:  Valeria Ricotti; Herbert Jägle; Maria Theodorou; Anthony T Moore; Francesco Muntoni; Dorothy A Thompson
Journal:  Eur J Hum Genet       Date:  2015-06-17       Impact factor: 4.246

2.  Intellectual ability in the duchenne muscular dystrophy and dystrophin gene mutation location.

Authors:  V Milic Rasic; D Vojinovic; J Pesovic; G Mijalkovic; V Lukic; J Mladenovic; A Kosac; I Novakovic; N Maksimovic; S Romac; S Todorovic; D Savic Pavicevic
Journal:  Balkan J Med Genet       Date:  2015-04-10       Impact factor: 0.519

Review 3.  Learning disabilities in neuromuscular disorders: a springboard for adult life.

Authors:  Guja Astrea; Roberta Battini; Sara Lenzi; Silvia Frosini; Silvia Bonetti; Elena Moretti; Silvia Perazza; Filippo M Santorelli; Chiara Pecini
Journal:  Acta Myol       Date:  2016-10

Review 4.  The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review.

Authors:  S Ryder; R M Leadley; N Armstrong; M Westwood; S de Kock; T Butt; M Jain; J Kleijnen
Journal:  Orphanet J Rare Dis       Date:  2017-04-26       Impact factor: 4.123

5.  Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophy.

Authors:  Amel Saoudi; Faouzi Zarrouki; Catherine Sebrié; Charlotte Izabelle; Aurélie Goyenvalle; Cyrille Vaillend
Journal:  Dis Model Mech       Date:  2021-09-21       Impact factor: 5.758

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.