Opitz GBBB syndrome
ORPHA:2745· ICD-10 Q87.8
Definition
A rare X-linked congenital midline malformation syndrome characterized by hypertelorism, laryngo-tracheo-esophageal defects and hypospadias.
- Prevalence
- Unknown
- Inheritance
- X-linked recessive
- Age of onset
- Antenatal, Infancy, Neonatal