“…Other specific, but less frequent, types include genetic defects of beta cell function (MODY, or maturity-onset diabetes of the young, and MIDD, or maternally inherited diabetes and deafness), genetic defects of insulin action, diseases of the exocrine pancreas, endocrinopathies, drug-or chemical-induced dia-betes, infections, immune-mediated diabetes, other genetic syndromes (Down syndrome, Klinefelter's syndrome, Turner's syndrome, Wolfram syndrome, Friedreich's ataxia, Huntington's chorea, Lawrence-Moon-Biedl syndrome, and myotonic dystrophy, among others), 1,3-6 and gestational diabetes. 21 This condition can bring about endolymph retention, hydrops, and auditory alterations. The most common mutation occurs at position 3243 in the tRNA leucine gene.…”