Cochlear implantation in a patient with profound hearing loss with the A1555g mitochondrial mutation

American Journal of Otology

Volumn 19, Issue 6, 1998, Pages 754-757

  Tono, Tetsuya ^a   Ushisako, Yasuaki ^a   Kiyomizu, Kensuke ^a   Usami, Shin Ichi ^b   Abe, Satoko ^b   Shinkawa, Hideichi ^b   Komune, Shizuo ^a  

^a UNIVERSITY OF MIYAZAKI   (Japan)

^b HIROSAKI UNIVERSITY   (Japan)

Author keywords

Cochlear implant; Mitochondrial mutation; Ototoxicity; Sensorineural hearing loss; Streptomycin

Indexed keywords

STREPTOMYCIN;

ADULT; ARTICLE; AUDIOMETRY; CASE REPORT; COCHLEA PROSTHESIS; HAIR CELL; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGNOSIS; STRIA VASCULARIS; VERTICAL TRANSMISSION;

EID: 0031765087     PISSN: 01929763     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Prezant TR, Agapian JV, Bohlman MC, et al. Mitochondrial ribosomal RNA mutation associated with both antibiotic induced and non-syndromic deafness. Nat Genet 1993;4:289-93.
2. Fichel-Ghodsian N, Prezant TR, Bu X, et al. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Otolaryngol 1993;14:399-403.
3. Hutchin T, Haworth J, Higashi K, et al. A molecular basis for human hypersensitivity to aminoglycoside antibiotics. Nucleic Acids Res 1993;21:4174-9.
4. Usami S, Abe S, Kasai M, et al. Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation. Laryngoscope 1997;107:483-90.
5. Huizing EH, de Groot JCMJ. Human cochlear pathology in aminoglycoside ototoxicity - a review. Acta Otolaryngol 1987;436: 117-25.
6. Garetz SL, Schacht J. Ototoxicity: of mice and men. In: Van De Water TR, Popper AN, Fay RR, eds. Clinical aspects of hearing. New York: Springer-Verlag, 1996:116-54.
7. Anniko M. Principles in cochlear toxicity. Arch Toxicol 1985;8:221-39.
8. Oshima T, Ueda N, Ikeda K, et al. Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome. Laryngoscope 1996;106:46-8.
9. Yamasoba T, Yoshimoto O, Tsukuda K, et al. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNALeu(UUR) Gene. Laryngoscope 1996;106:49-53.
10. Sawada S, Takeda T, Kakigi A, et al. Audiological findings of sensorineural deafness associated with a mutation in the mitochondrial DNA. Am J Otol 1997;18:332-5.
11. Marangos N, Mausolf A. Familiare Neural Mitochondriale Shwerhorigkeit. HNO 1990;38:322-5.
12. Elverland HH, Torbergsen T. Audiologic findings in a family with mitochondrial disorder. Am J Otol 1991;12:459-65.
13. Lupo I, Ciulla L, Cusimano F, et al. Brainstem auditory evoked potentials in patients with mitochondrial encephalomyopathy. Acta Neurol (Napoli) 1992;14:163-72.
14. Lindsay JR, Hinojosa R. Histopathological features of the inner ear associated with Kearns-Sayre syndrome. Arch Otolaryngol Head Neck Surg 1976;102:747-52.
15. Yamaguchi T, Himi T, Harabuchi Y, et al. Cochlear implantation in a patient with mitochondrial disease - Kearns-Sayre syndrome: a case report. In: Honjo I, Takahashi H, eds. Cochlear implant and related sciences update. Adv Otorhinolaryngol. Basel: Karger, 1997;52:321-3.