双皮质素基因突变所致无脑回畸形I型
ORPHA:2148· ICD-10 Q04.3· Lissencephaly type 1 due to doublecortin gene mutation
- 患病率
- Unknown
- 遗传方式
- X-linked recessive
- 发病年龄
- Adolescent, Childhood, Infancy, Neonatal
ORPHA:2148· ICD-10 Q04.3· Lissencephaly type 1 due to doublecortin gene mutation