Síndrome asociado a una variante patogénica del gen SATB2
ORPHA:576283· ICD-10 Q87.8· SATB2-associated syndrome due to a pathogenic variant
- Herencia
- Autosomal dominant
- Edad de inicio
- Antenatal, Infancy, Neonatal
ORPHA:576283· ICD-10 Q87.8· SATB2-associated syndrome due to a pathogenic variant