This article presents a detailed case report of a patient who was diagnosed with superior canal dehiscence at 37 years of age, but who had a suspicious history for that syndrome from at least 10 years of age. The authors hypothesize several reasons for this late diagnosis, with the goal of helping pediatricians, otolaryngologists, and neurologists consider this syndrome in their differential diagnosis of children, adolescents, or adults experiencing dizziness.
AbstractSuperior canal dehiscence syndrome (SCDS) is typically diagnosed in adulthood and not in children or adolescents, but it is believed that it is caused by a developmental or congenital anomaly. This theory would predict more diagnoses earlier in live, but until now the facts do not show that. We report a patient, in whom the diagnosis was made at age 37 but who had a suspicious history for that syndrome from at least age 10. We hypothesize some reasons for this late diagnosis and hope this case may have the effect, to make even pediatricians, ENT-doctors and neurologists seeing children think at this syndrome and to help some of their patients, to have a better live.