Abstract
• Hearing function and auditory brainstem potentials were evaluated in nine members of three generations of a family affected with Friedreich's ataxia. The characteristic findings were high-frequency sensorineural hearing impairment of varying severity and diminished or absent N1, N2, and N3 responses. These electrophysiologic aberrations correlate topographically with previously reported pathological observations. (Arch Otolaryngol 1981;107:254-256).
| Original language | English |
|---|---|
| Pages (from-to) | 254-256 |
| Number of pages | 3 |
| Journal | Archives of Otolaryngology |
| Volume | 107 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 1981 |
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