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. 2017 Jan 19;7:34425. doi: 10.1038/srep34425

Table 1. Summary of clinical data for the hearing-impaired members of Family 304.

Subject Gendera Age of test (year) Age of onset (year) PTA (dB HL)b Hearing impairmentc Audiogram Tinnitus Vertigo Mutationd detected
III:2 F 57 Not clear L:71.25 Severe Downslope + c. 524C > A
        R:67.5 Moderately severe Downslope      
III:3 M 60 N/A L:32.50 Mild Downslope
        R:30.00 Mild Downslope      
III:8 F 50 23 L:76.25 Severe Downslope + c. 524C > A
        R:77.50 Severe Downslope      
III:10 F 49 21 L:75.00 Severe Downslope + c. 524C > A
        R:98.75 Profound Downslope      
III:5 M 55 N/A L:32.50 Mild U-shape
        R:42.50 Moderate U-shape      
III:12 F 47 0 L:>100 Profound Flat + c. 524C > A
        R:66.25 Moderately severe Downslope      
III:14 F 44 42 L:21.25 Normal U-shape
        R:21.25 Normal U-shape      
III:16 F 43 0 L:77.50 Severe Downslope c. 524C > A
        R:81.25 Severe Downslope      
III:18 F 39 0 L:68.33 Moderately severe Downslope + c. 524C > A
        R:>100 Profound Flat      
IV:2 M 35 Not clear L:78.75 Severe Downslope + c. 524C > A
        R:90.00 Severe Downslope      
IV:3 F 30 Not clear L:53.75 Moderate Downslope + c. 524C > A
        R:50.00 Moderate Downslope      
IV:6 M 30 N/A L:38.75 Mild U-shape -
        R:40.00 Mild U-shape      
IV:12 M 24 0 L:72.50 Severe Downslope + c. 524C > A
        R:73.75 Severe Downslope      
IV:13 F 24 Not clear L:43.75 Moderate Downslope + c. 524C > A
        R:53.75 Moderately severe Downslope      
IV:20 F 2 0 L:110dBnHL Profound / c. 524C > A
        R:90dBnHL Profound /      
IV:21 F 14 0 L:70.00 Moderately severe Downslope + c. 524C > A/c.235delC
        R:71.25 Severe Downslope      

N/A, not available; +, positive finding; −, negative finding.

aM, male; F, female.

bPTA, pure-tone air-conduction averages (0.5, 1, 2 and 4 kHz). L, left ear, R, right ear. For the IV:20, who was 2 years old, her thresholds were the results of 40Hz AERP (auditory event-related potential) by tone burst.

cDiagnosed at the time of test.

dRefSeq: NM_004004, GRCh37/hg19 chr13.