Congenital hereditary facial paralysis-variable hearing loss syndrome is an extremely rare autosomal recessive disorder characterized by bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears), and strabismus. The disease is congenital hereditary facial paralysis-variable hearing loss syndrome (MONDO_0017627). Also known as: congenital hereditary facial palsy with variable deafness, congenital hereditary facial palsy with variable hearing loss, congenital hereditary facial paralysis with variable deafness, congenital hereditary facial paralysis-variable deafness syndrome.