Shprintzen-Goldberg sendromu
ORPHA:2462· ICD-10 Q87.8· Shprintzen-Goldberg syndrome
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal dominant, Multigenic/multifactorial, Not applicable
- Başlangıç yaşı
- Antenatal, Infancy, Neonatal
ORPHA:2462· ICD-10 Q87.8· Shprintzen-Goldberg syndrome