母源染色体14q32.2微缺失所致加Kagami-Ogata综合征
ORPHA:254528· ICD-10 Q93.5· Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal dominant, Not applicable
- 发病年龄
- Infancy, Neonatal
ORPHA:254528· ICD-10 Q93.5· Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion