遗传性包涵体肌病-关节挛缩-眼肌麻痹综合征
ORPHA:79091· ICD-10 G71.8· Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal dominant
- 发病年龄
- Adolescent, Infancy, Neonatal
ORPHA:79091· ICD-10 G71.8· Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome