Assessment of ventricular repolarization in deaf-mute children

The long QT syndrome is a congenital disease with frequent familial transmi ssion, characterized primarily by prolongation of the QT interval and by th e occurrence of life-threatening arrhythmias. The syndrome may be familial, with or without congenital deafness, or it may be idiopathic. We attempted to assess ventricular repolarization and to identify patients with the Jer vell and Lange-Nielsen syndrome among 132 deaf-mute school children. Five d eaf-mute subjects had Jervell and Lange-Nielsen syndrome. The deaf-mute sub jects were divided into two subgroups according to the length of their QT i ntervals: group 1 included 5 cases with the long QT interval (>440 msec), a nd group 2 included 127 subjects with the normal QT interval (less than or equal to 440 msec). Group 3 was composed of 96 control subjects. The mean Q T, QTc, JT, and JTc intervals (418 +/- 70, 500 +/- 38, 302 +/- 65, and 389 +/- 36 msec, respectively) in group 1 were significantly longer than those of group 2 (344 +/- 23, 408 +/- 22, 249 +/- 34, and 291 +/- 28 msec, respec tively) and group 3 (325 +/- Il, 383 +/- 26, 228 +/- 36, and 269 +/- 46 mse c, respectively). The dispersion (d) values (QT-d, QTc-d, JT-d, and JTc-d; 63 +/- 10, 73 +/- 8, 60 +/- 8, and 62 +/- Il msec, respectively) of group 1 were significantly longer than those of group 2 (49 +/- 16, 43 +/- 11, 48 +/- 21, and 45 +/- 18 msec, respectively) and group 3 (33 +/- 13, 33 +/- 14 , 28 +/- 16, and 27 +/- 14 msec, respectively) at similar mean RR intervals . Also, the mean QT, QTc, JT, and JTc intervals and the dispersion values ( QT-d, QTc-d, JT-d, and JTc-d) in group 2 were significantly longer than tho se of group 3 at similar mean RR intervals. Consequently, in this study, we determined that the deaf-mute children who did not meet the criteria for J ervell and Lange-Nielsen syndrome still had evidence of subtle derepolariza tion abnormalities evidenced by intermediate prolongation of QTc, JTc, and the corresponding measures of dispersion, and we believe an electrocardiogr am examination of deaf-mute subjects will reveal this potentially life-thre atening syndrome.