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Interpretation of 'Diagnosis and management of Duchenne muscular dystrophy: a guide for families (2011 version)'

机译:解读“杜兴氏肌营养不良症的诊断和处理:家庭指南(2011年版)”

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The guideline "Diagnosis and management of Duchenne muscular dystrophy" was supported by a 3-year-long project guided by US Centers for Disease Control and Prevention (CDC), in collaboration with patient advocacy groups [Muscular Dystrophy Association (MDA), Parent Project Muscular Dystrophy (PPMD) and United Parent Projects Muscular Dystrophy (UPPMD)] and Translational Research in Europe: Assessment and Treatment of Neuromuscular Disease (TREAT-NMD) network. The main document was published in Lancet Neurol in 2010. The recommendations are based on an extensive study by 84 international experts in Duchenne muscular dystrophy (DMD) diagnosis and care who were chosen to represent a broad range of specialties. This guideline covers diagnostics, steroid treatment, rehabilitation, orthopedics, pulmonary, cardiac, gastrointestinal, psychosocial, surgical and emergency management of DMD. This guideline is recommended as the first choice by TREAT- NMD for DMD diagnosis and care.?DOI: 10.3969/j.issn.1672-6731.2015.05.003.
机译:指南“杜兴氏肌营养不良症的诊断和管理”得到了美国疾病控制与预防中心(CDC)与患者倡导团体[肌肉营养不良协会(MDA)的父项目肌营养不良症(PPMD)和美国父母项目肌营养不良症(UPPMD)]和欧洲转化研究:神经肌肉疾病的评估和治疗(TREAT-NMD)网络。主要文档于2010年在《柳叶刀》《神经病学》上发表。这些建议是基于84位国际杜兴氏肌营养不良(DMD)诊断和护理专家的广泛研究得出的,他们被选为代表广泛的专业。本指南涵盖DMD的诊断,类固醇治疗,康复,骨科,肺,心脏,胃肠道,社会心理,外科手术和急诊管理。 TREAT-NMD建议将此指南作为DMD诊断和护理的首选。DOI:10.3969 / j.issn.1672-6731.2015.05.003。

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