关节挛缩-眼球运动受限-电传导异常综合征
ORPHA:1154· ICD-10 Q68.8· Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome
- 患病率
- Unknown
- 遗传方式
- Autosomal dominant, Autosomal recessive
- 发病年龄
- Neonatal
ORPHA:1154· ICD-10 Q68.8· Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome