The autoimmune inner ear disease is a rare case of reversible sensorioneural hearing loss. The typical afflicted patient is the middle-aged woman, and it is very rare in the pediatric population. The diagnosis is based on disease manifestations, laboratory exams and a positive corticosteroid response. The audiometric evaluation does not revel typical characteristics. The authors report a case of autoimmune sensorioneural hearing loss in a seven-year-old child.
autoimmune sensorioneural hearing loss; inner ear; children