Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy

<p>Duchenne muscular dystrophy (DMD), clinically featured as progressive skeletal muscle atrophy with gradual loss of muscle strength and activity abilities, is the most common genetic muscular disease in children throughout the world. The core and continuous characteristic of DMD is motor dys...

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Main Author: Wei SHI
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2015-06-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/1206
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spelling doaj-246c78f40aea45aa8a81fd6c1ebb88982020-11-24T23:01:49ZengTianjin Huanhu HospitalChinese Journal of Contemporary Neurology and Neurosurgery1672-67312015-06-011564264311197Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophyWei SHI0Rehabilitation Center, Children's Hospital of Fudan University, Shanghai 201102, China<p>Duchenne muscular dystrophy (DMD), clinically featured as progressive skeletal muscle atrophy with gradual loss of muscle strength and activity abilities, is the most common genetic muscular disease in children throughout the world. The core and continuous characteristic of DMD is motor dysfunction. Motor function assessments of DMD are now focusing on muscle strength, walking ability, range of motion and ability of activities, still without unified standards. Confirming the comprehensive, scientific, reasonable and accurate evaluation tools for DMD assessment is the premise of research in motor developmental rules of DMD, which will help to better understand the motor progress of DMD and to supply evidences for choosing treatment methods, confirming timing of intervention, assessing effect of treatments and designing rehabilitation plans.</p><p> </p><p><strong>DOI: </strong>10.3969/j.issn.1672-6731.2015.06.002</p>http://www.cjcnn.org/index.php/cjcnn/article/view/1206Muscular dystrophy, DuchenneMovement disordersReview
collection DOAJ
language English
format Article
sources DOAJ
author Wei SHI
spellingShingle Wei SHI
Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
Chinese Journal of Contemporary Neurology and Neurosurgery
Muscular dystrophy, Duchenne
Movement disorders
Review
author_facet Wei SHI
author_sort Wei SHI
title Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
title_short Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
title_full Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
title_fullStr Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
title_full_unstemmed Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
title_sort research progress of motor function assessments and their clinical applications in duchenne muscular dystrophy
publisher Tianjin Huanhu Hospital
series Chinese Journal of Contemporary Neurology and Neurosurgery
issn 1672-6731
publishDate 2015-06-01
description <p>Duchenne muscular dystrophy (DMD), clinically featured as progressive skeletal muscle atrophy with gradual loss of muscle strength and activity abilities, is the most common genetic muscular disease in children throughout the world. The core and continuous characteristic of DMD is motor dysfunction. Motor function assessments of DMD are now focusing on muscle strength, walking ability, range of motion and ability of activities, still without unified standards. Confirming the comprehensive, scientific, reasonable and accurate evaluation tools for DMD assessment is the premise of research in motor developmental rules of DMD, which will help to better understand the motor progress of DMD and to supply evidences for choosing treatment methods, confirming timing of intervention, assessing effect of treatments and designing rehabilitation plans.</p><p> </p><p><strong>DOI: </strong>10.3969/j.issn.1672-6731.2015.06.002</p>
topic Muscular dystrophy, Duchenne
Movement disorders
Review
url http://www.cjcnn.org/index.php/cjcnn/article/view/1206
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