Profile of cognitive function in adults with duchenne muscular dystrophy

被引:10
|
作者
Ueda, Yukihiko [1 ]
Suwazono, Shugo [2 ]
Maedo, Sino [1 ]
Higuchi, Itsuro [3 ]
机构
[1] Okinawa Int Univ, Ginowan 2-6-1, Ginowan, Okinawa, Japan
[2] Natl Hosp Org, Okinawa Natl Hosp, Ginowan, Okinawa, Japan
[3] Kagoshima Univ, Fac Med, Sch Hlth Sci, Kagoshima, Kagoshima, Japan
来源
BRAIN & DEVELOPMENT | 2017年 / 39卷 / 03期
关键词
Duchenne muscular dystrophy; Cognitive function; Neuropsychological profile; Sequential processing; DEFICIT HYPERACTIVITY DISORDER; SHORT FORMS; IMPAIRMENT; BOYS; INTELLIGENCE; ASSOCIATION; CHILDREN; ATROPHY;
D O I
10.1016/j.braindev.2016.10.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Several studies have examined intellectual functioning of boys with duchenne muscular dystrophy (DMD). However, little is known about the remaining cognitive weaknesses in adults with DMD. Objective: The purpose of this study was to investigate the profile of cognitive functioning that is characteristics of adults with DMD. Methods: Twenty-four subscales from the Wechsler Adult Intelligence Scale III (WAIS-III), the Clinical Assessment for Attention (CAT), and the Wechsler Memory Scale Revised (WMS-R) were used to assess participants with DMD (N = 15; mean age = 30.4 years). Results: Scores for Picture Completion, Arithmetic, Matrix Reasoning, Symbol Search, Letter-Number Sequencing, and Digit Span of the WAIS-III; all CAT scores, and Logical Memory and Delayed Logical Memory from the WMS-R were significantly deficient in adults with DMD in comparison to the normal population. Conclusion: The ability to sequentially process auditory and visual information remains impaired in adults with DMD. (C) 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 230
页数:6
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