Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
ORPHA:2250· ICD-10 Q87.0
Definition
This syndrome is characterized by the association of severe nasal hypoplasia, hypoplasia of the eyes, hyposmia, hypogeusia and hypogonadotropic hypogonadism.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant, Unknown
- Age of onset
- Antenatal, Neonatal