Research progress of motor function assessments and their clinical applications in Duchenne muscular dystrophy
Autor: | Wei SHI |
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Sprache: | Englisch; Chinesisch |
Veröffentlicht: |
2015 |
Quelle: | Directory of Open Access Journals: DOAJ Articles |
Online Zugang: |
http://www.cjcnn.org/index.php/cjcnn/article/view/1206 https://doaj.org/toc/1672-6731 1672-6731 https://doaj.org/article/246c78f40aea45aa8a81fd6c1ebb8898 https://doaj.org/article/246c78f40aea45aa8a81fd6c1ebb8898 |
Erfassungsnummer: | ftdoajarticles:oai:doaj.org/article:246c78f40aea45aa8a81fd6c1ebb8898 |
Zusammenfassung
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. DOI: 10.3969/j.issn.1672-6731.2015.06.002