睑裂-智力障碍综合征
ORPHA:293642· Blepharophimosis-intellectual disability syndrome
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, X-linked recessive
- 发病年龄
- Infancy, Neonatal
ORPHA:293642· Blepharophimosis-intellectual disability syndrome