Shprintzen-Goldberg综合症
ORPHA:2462· ICD-10 Q87.8· Shprintzen-Goldberg syndrome
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal dominant, Multigenic/multifactorial, Not applicable
- 发病年龄
- Antenatal, Infancy, Neonatal
ORPHA:2462· ICD-10 Q87.8· Shprintzen-Goldberg syndrome