脊髓灰质炎后进行性肌萎缩
Post polio progressive muscular atrophy
- 上级条目
- 运动神经元疾病或相关疾患
- 层级
- 3 级
定义
脊髓灰质炎后进行性肌萎缩（PPMA）的诊断标准是：有可靠的脊髓灰质炎病史，功能部分恢复，至少10年稳定期，随后发展为进行性肌无力。以前受累的肌肉可能出现虚弱、萎缩和疲劳的症状。这些症状也可能在明显未受脊髓灰质炎影响的肌肉中新出现。肌肉痉挛和肌束震颤可能伴随着新的无力。
The diagnostic criteria for Post-polio progressive muscular atrophy (PPMA) are: a credible history of poliomyelitis with partial recovery of function, a minimum 10-year period of stabilization, and the subsequent development of progressive muscle weakness. Symptoms of weakness, atrophy, and fatigue of previously affected muscles may be seen. These symptoms may also be newly noted in muscles that were apparently unaffected by the poliomyelitis episode. Muscle cramps and fasciculations may accompany the new weakness.
包含词 该编码包含的临床情况，通常不作为独立编码
- 脊髓灰质炎后综合征
英文词条（1）
- post polio myelitic syndrome
索引词 可用于检索该条目的同义词与别名
- 脊髓灰质炎后进行性肌萎缩
- 脊髓灰质炎后综合征
- PPMA[脊髓灰质炎后进行性肌萎缩]
- post polio myelitic syndrome [No translation available]
- 脊髓灰质炎后综合征
英文词条（4）
- Post polio progressive muscular atrophy
- PPMA - [post polio progressive muscular atrophy]
- post polio myelitic syndrome
- post polio syndrome
后组配轴 Postcoordination
后组配是在主干编码之后追加的可选扩展轴（如侧别、具体解剖部位、严重程度），用于把「部位 + 侧别 + 病程」等细节一次表达完整。只有标注「必填」的轴在组合编码时必须给出，其余可留空。
- 临床表现hasManifestation可选