腓骨肌萎缩症/遗传性运动感觉性神经病
ORPHA:166· Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy
- 患病率
- 1-5 / 10 000
- 遗传方式
- Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive
- 发病年龄
- All ages
ORPHA:166· Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy