Literature DB >> 2310438

Etiology of intellectual impairment in Duchenne muscular dystrophy.

A A al-Qudah1, J Kobayashi, S Chuang, M Dennis, P Ray.   

Abstract

The precise etiology of intellectual impairment in Duchenne muscular dystrophy (DMD) is unknown. Histopathologic and computed tomographic studies have revealed structural brain changes; however, to our knowledge, no cranial magnetic resonance imaging (MRI) studies have been performed on DMD patients to further delineate these structural changes. We prospectively studied 4 DMD patients by cranial MRI, DNA deletion analysis, clinical evaluation, and intelligence testing. There was no significant correlation between verbal intelligence scores and MRI findings, DNA deletion, or the clinical severity of the disease. These first MRI studies of DMD did not reveal any significant anatomic brain alteration, other than mild atrophy in 2 patients. We believe these results must be considered when investigating the etiology of intellectual impairment in DMD in future studies with larger patient samples.

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Year:  1990        PMID: 2310438     DOI: 10.1016/0887-8994(90)90081-b

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  7 in total

Review 1.  Cognitive dysfunction in Duchenne muscular dystrophy: a possible role for neuromodulatory immune molecules.

Authors:  Mark G Rae; Dervla O'Malley
Journal:  J Neurophysiol       Date:  2016-07-06       Impact factor: 2.714

2.  Diffusion tensor imaging study in Duchenne muscular dystrophy.

Authors:  Ya Fu; Yuru Dong; Chao Zhang; Yu Sun; Shu Zhang; Xuetao Mu; Hong Wang; Weihai Xu; Shiwen Wu
Journal:  Ann Transl Med       Date:  2016-03

3.  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

4.  Psychological aspects in children affected by duchenne de boulogne muscular dystrophy.

Authors:  Teresa Di Filippo; Lucia Parisi; Michele Roccella
Journal:  Ment Illn       Date:  2014-03-19

Review 5.  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 6.  The roles of the dystrophin-associated glycoprotein complex at the synapse.

Authors:  Gonneke S K Pilgram; Saranyapin Potikanond; Richard A Baines; Lee G Fradkin; Jasprina N Noordermeer
Journal:  Mol Neurobiol       Date:  2009-11-09       Impact factor: 5.590

7.  Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy.

Authors:  Bauke Kogelman; Artem Khmelinskii; Ingrid Verhaart; Laura van Vliet; Diewertje I Bink; Annemieke Aartsma-Rus; Maaike van Putten; Louise van der Weerd
Journal:  PLoS One       Date:  2018-03-30       Impact factor: 3.240

  7 in total

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