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BICD2基因相关儿童起病常染色体显性近端脊髓性肌萎缩症

ORPHA:363454· ICD-10 G12.1· BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy

患病率
<1 / 1 000 000
遗传方式
Autosomal dominant
发病年龄
Antenatal, Childhood, Infancy, Neonatal