Literature DB >> 24279481

Neuropsychological profile of duchenne muscular dystrophy.

Anna Roshini Perumal1, Jamuna Rajeswaran, Atchayaram Nalini.   

Abstract

Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder characterized by progressive muscle wasting. DMD is a fatal X-linked recessive disorder with an estimated prevalence of 1 in 3,500 male live births. This disease has long been associated with intellectual impairment. Research has shown that boys with DMD have variable intellectual performance, indicating the presence of specific cognitive deficits. The aim of the study was to use a battery of intelligence, learning, and memory tests to identify a neuropsychological profile in boys with DMD. A total of 22 boys diagnosed with DMD in the age range of 6 to 10 years old were evaluated using the Wechsler Intelligence Scale for Children-Third Edition, Rey's Auditory Verbal Learning Test, and the Memory for Designs Test. The data were interpreted using means, standard deviations, percentages, and percentiles. Normative data were also used for further interpretation. The results showed that boys with DMD had a significantly lower IQ (88.5). Verbal IQ (86.59) was found to be lower than Performance IQ (92.64). There was evidence of impaired performance on the Processing Speed, Freedom From Distractibility, and Verbal Comprehension Indexes. Specific deficits in information processing, complex attention, immediate verbal memory span, verbal working memory, verbal comprehension, vocabulary, visuoconstruction ability, and verbal learning and encoding were observed. However, perceptional organization, general fund of information, abstract reasoning, visual discrimination and acuity, visual learning and memory, and verbal memory were adequate. The neuropsychological findings support the hypothesis that these children have specific cognitive deficits as opposed to a global intellectual deficit.

Entities:  

Keywords:  cognitive functions; duchenne muscular dystrophy; intelligence; neuropsychological profile

Mesh:

Year:  2013        PMID: 24279481     DOI: 10.1080/21622965.2013.802649

Source DB:  PubMed          Journal:  Appl Neuropsychol Child        ISSN: 2162-2965            Impact factor:   1.493


  6 in total

Review 1.  Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Susan D Apkon; Angela Blackwell; Mary K Colvin; Linda Cripe; Adrienne R Herron; Annie Kennedy; Kathi Kinnett; James Naprawa; Garey Noritz; James Poysky; Natalie Street; Christina J Trout; David R Weber; Leanne M Ward
Journal:  Lancet Neurol       Date:  2018-02-02       Impact factor: 44.182

Review 2.  Dystrophin induced cognitive impairment: mechanisms, models and therapeutic strategies.

Authors:  Akshay Anand; Rahul Tyagi; Manju Mohanty; Manoj Goyal; K Ranil D De Silva; Nalaka Wijekoon
Journal:  Ann Neurosci       Date:  2015-04

3.  Computational cognitive modeling and validation of Dp140 induced alteration of working memory in Duchenne Muscular Dystrophy.

Authors:  Rahul Tyagi; Palvi Aggarwal; Manju Mohanty; Varun Dutt; Akshay Anand
Journal:  Sci Rep       Date:  2020-07-20       Impact factor: 4.379

4.  Mitochondrial Dysfunction Is an Early Consequence of Partial or Complete Dystrophin Loss in mdx Mice.

Authors:  Timothy M Moore; Amanda J Lin; Alexander R Strumwasser; Kevin Cory; Kate Whitney; Theodore Ho; Timothy Ho; Joseph L Lee; Daniel H Rucker; Christina Q Nguyen; Aidan Yackly; Sushil K Mahata; Jonathan Wanagat; Linsey Stiles; Lorraine P Turcotte; Rachelle H Crosbie; Zhenqi Zhou
Journal:  Front Physiol       Date:  2020-06-19       Impact factor: 4.566

5.  Working Memory Alterations Plays an Essential Role in Developing Global Neuropsychological Impairment in Duchenne Muscular Dystrophy.

Authors:  Rahul Tyagi; Harshita Arvind; Manoj Goyal; Akshay Anand; Manju Mohanty
Journal:  Front Psychol       Date:  2021-01-15

Review 6.  The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic.

Authors:  Aravindhan Veerapandiyan; Kathryn R Wagner; Susan Apkon; Craig M McDonald; Katherine D Mathews; Julie A Parsons; Brenda L Wong; Katy Eichinger; Perry B Shieh; Russell J Butterfield; Vamshi K Rao; Edward C Smith; Crystal M Proud; Anne M Connolly; Emma Ciafaloni
Journal:  Muscle Nerve       Date:  2020-05-05       Impact factor: 3.852

  6 in total

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