线粒体和过氧化物酶体裂变缺陷所致DNM1L相关脑病
ORPHA:330050· ICD-10 E88.8· DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal dominant
- 发病年龄
- Childhood, Infancy, Neonatal
ORPHA:330050· ICD-10 E88.8· DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect