8C75
远端肌病
Distal myopathies
- 上级条目
- 原发性肌肉功能障碍
- 层级
- 4 级
定义
远端型肌病是一组异质性肌病，其临床特征为从远端肌肉开始的进行性无力和萎缩，组织学特征为肌肉活检的非特异性肌病特征。
Distal myopathies are heterogeneous group of myopathies characterised clinically by progressive weakness and atrophy starting in distal muscles and progressing to proximal ones, and histologically by nonspecific myopathic features on muscle biopsy.
索引词 可用于检索该条目的同义词与别名
- 远端肌病
- 远端型肌营养不良
- 胫前肌发病的远端肌病
- Markesbery-Griggs远端肌病
- 胫骨肌肉萎缩症 [possible translation]
- 胫骨肌肉萎缩症
- 远端肌病伴早期呼吸肌受累
- 远端肌病伴腿后部或手前部受累
- 远端肌病伴声带无力
- 远端肌病伴镶边空泡
- Nonaka肌病
- Welander远端肌病
- WDM – [Welander远端型肌病]
- Laing远端肌病
- 远端肌病，Miyoshi型
- 胫骨肌营养不良，Udd型
- 某些特指的罕见远端肌病
英文词条（16）
- Distal myopathies
- Distal muscular dystrophy
- Distal myopathy with anterior tibial onset
- Markesbery-Griggs distal myopathy
- Tibial muscular dystrophy
- Distal myopathy with early respiratory muscle involvement
- Distal myopathy with posterior leg or anterior hand involvement
- Distal myopathy with vocal cord weakness
- Distal myopathy with rimmed vacuoles
- Nonaka myopathy
- Welander distal myopathy
- WDM – [Welander distal myopathy]
- Laing distal myopathy
- Distal myopathy, Miyoshi type
- Tibial muscular dystrophy, Udd type
- Certain specified rare distal myopathy
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。