脑肌病型线粒体DNA缺失综合征伴肾小管病变
ORPHA:255235· ICD-10 G31.8· Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Infancy, Neonatal
ORPHA:255235· ICD-10 G31.8· Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy