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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Tianjin Huanhu Hospital
2015-06-01
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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 |
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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 |
work_keys_str_mv |
AT weishi researchprogressofmotorfunctionassessmentsandtheirclinicalapplicationsinduchennemusculardystrophy |
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