This syndrome is characterized by the association of severe nasal hypoplasia, hypoplasia of the eyes, hyposmia, hypogeusia and hypogonadotropic hypogonadism. The disease is Orphanet rare-disease nomenclature id Orphanet_2250 (Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism). Also known as: Bosma-Henkin-Christiansen syndrome.