Audiologic evaluation in a family showing diabetes mellitus and deafness associated with a mutation in mitochondrial DNA

Abstract

An A to G transition at nucleotide 3, 243 in the tRNALeu(UUR) gene of mitochondrial DNA has recently been identified as a pathogenic point mutation which is associated with diabetes mellitus and sensorineural deafness in several pedigrees. We have also reported a family showing the association of deafness and diabetes mellitus as the predominant clinical features with this mutation. Audiologic data from two patients in this family are presented. Both had a bilaterally symmetrical sensorineural hearing loss at all frequencies. As is often the case with deafness associated with a mitochondrial disorder, the pure-tone threshold values were maximal at high frequencies in both patients. The audiologic work-up presented not only cochlear characteristics but also signs suggestive of retrocochlear disturbance with poor speech discrimination scores as compared to pure-tone thresholds, although auditory brain-stem responses showed neither wave delay nor prolonged interpeak latencies. Caloric excitability was not impaired. © 1995, The Oto-Rhino-Laryngological Society of Japan, Inc. All rights reserved.