Abstract :
Wilderwanck syndrome is a rare congenital disorder involving the neck, eyes and the hearing. It is characterised by a triad of symptoms, including Duane retraction syndrome, Klippel-Feil syndrome and Hearing loss. The original description of WS included sensori neural hearing loss. We describe a case of a 24-year-old female with Klippel-feil anamoly, Duane syndrome type 3 and mixed hearing loss, with unilateral congenital malformation of the inner ear.
Keyword :
Wilderwanck Syndrome, Mixed Hearing loss, Conductive hearing loss, Mondini's anamoly