线粒体和过氧化物酶体分裂缺陷导致的MFF相关性脑病
ORPHA:485421· ICD-10 E88.8· MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Infancy
ORPHA:485421· ICD-10 E88.8· MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect