An extremely rare autosomal recessive disorder with characteristics of bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears) and strabismus.
syndrome de paralysie faciale congénitale héréditaire-surdité variable
SNOMEDCT-BE (midfacial retrusion, low-set ears) and strabismus. / 722389002
SNOMEDCT-BE (disorder) / 722389002