Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-29T13:24:32.638Z Has data issue: false hasContentIssue false

Alport's syndrome: audiological manifestations and implications

Published online by Cambridge University Press:  29 June 2007

M. J. Gleeson*
Affiliation:
London
*
Department of Otolaryngology, Derbyshire Royal Infirmary, Derby.

Abstract

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Research Article
Copyright
Copyright © JLO (1984) Limited 1984

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adhikary, H. P., Sells, R. A. and Basu, P. K. (1982) Ocular complications of systemic steroids after renal transplantation and their association with HLA. British Journal of Ophthalmology, 66: 290291.CrossRefGoogle ScholarPubMed
Alport, A. C. (1927) Hereditary familial congenital haemorrhagic nephritis. British Medical Journal, 1: 504506.CrossRefGoogle ScholarPubMed
Cassidy, G., Brown, K., Cohen, M., and De Mavia, W. (1965) Hereditary renal dysfunction and deafness. Paediatrics, 35: 967979.CrossRefGoogle Scholar
Cohen, M. M., Cassidy, G. and Hanna, B. L. (1961) A genetic study of hereditary renal dysfunction with associated nerve deafness. American Journal of Human Genetics, 13; 379389.Google ScholarPubMed
Drettner, B., Hedstrand, H., Klockhoff, I and Svedberg, A. (1975) Cardiovascular risk factors and hearing loss. Acta Otolaryngologica, 79: 366371.CrossRefGoogle ScholarPubMed
Efron, M. L. (1965) Familial hyperprolinaemia. New England Journal of Medicine, 272: 12431254.CrossRefGoogle Scholar
Hinglais, N., Gromfeld, J. L. & Bois, E. (1972) Characteristic ultrastructure lesion of the glomerular basement membrane in progressive hereditary nephritis (Alports Syndrome) Laboratory Investigation, 27: 473–87.Google Scholar
Hurst, A. F. (1923) Hereditary familial congenital haemorrhagic nephritis. Guy's Hospital Reports, 73: 368370.Google Scholar
Hutchinson, J. and Klodd, D. (1982) Electrophysiological analysis of auditory, vestibular and brainstem function in chronic renal failure. Laryngoscope, 92: 833843.CrossRefGoogle ScholarPubMed
Johnsson, D. W., and Mathog, R. H. (1976) Hearing function and chronic renal failure. Annals of Otology, Rhinology and Laryngology, 85: 4349.CrossRefGoogle Scholar
Johnsson, L.-G. and Arenberg, I. (1981) Cochlear abnormalities in Alports Syndrome. Archives of Otolaryngology, 107: 340349.CrossRefGoogle Scholar
McDonald, J. J., Zincke, H. and Anderson, C. F. (1978) Hearing loss improvement with transplantation. Laryngoscope, 88: 3842.CrossRefGoogle ScholarPubMed
Miller, G. W., Joseph, D. J., Cozad, R. L., and McCabe, B. F. (1970) Alports Syndrome. Archives of Otolaryngology, 92: 419432.CrossRefGoogle Scholar
Mitschke, H., Schmidt, P., Kopsa, H. and Zazgornik, J. (1975) Reversible hearing loss after transplantation. New England Journal of Medicine, 292: 10621063.CrossRefGoogle Scholar
Nakai, Y. (1977) Combined effect of 3', 4' dideoxykanamycin B. and potent diuretics on the cochlea. Laryngoscope, 87: 15481558.CrossRefGoogle ScholarPubMed
Oda, M.. Preciado, M., Quick, C. and Paparella, M. (1974) Labyrinthine pathology of chronic renal failure patients treated with haemodialysis and kidney transplantation. Laryngoscope, 84: 14891506.CrossRefGoogle ScholarPubMed
Perkoff, G. T., Stephens, F. E., Dolowitz, D. and Tyler, F. H. (1951) A clinical study of hereditary interstitial pyelonephritis. Archives of Internal Medicine, 88: 191200.CrossRefGoogle ScholarPubMed
Polak, B. C. (1980) Ophthalmological complications of haemodialysis and kidney transplants. Documenta Ophthalmologica, 49: 196.CrossRefGoogle Scholar
Prazma, J., Browder, J. P. and Fischer, N. D. (1974) Ethacrynic acid ototoxicity potentiation by Kanamycin. Annals of Otology, Rhinology and Laryngology, 83: 111118.CrossRefGoogle ScholarPubMed
Quick, C. A., Fish, A. and Brown, C. (1973) The relationship between the cochlea and kidney. Laryngoscope, 83: 14691482.CrossRefGoogle ScholarPubMed
Rintelmann, W. F. (1976) Auditory manifestations of Alports Disease Syndrome. Transactions of the Academy of Ophthalmology and Otolaryngology, 82: 375387.Google ScholarPubMed
Sohar, E. (1956) Renal disease, inner ear deafness and ocular changes: new heredofamilial syndrome. Archives of Internal Medicine, 97: 627630.Google ScholarPubMed
Spear, G. S., Whitworth, J. M. and Konigsmark, B. W. (1970) Hereditary nephritis with nerve deafness: Immunofluorescent studies on the kidney with consideration of discordant immunoglobulin—complement immunofluorescent reactions. American Journal of Medicine, 49: 5263.CrossRefGoogle ScholarPubMed
Tina, L. U., Lou, M. F., Dizio, D. and Caleagno, P. L. (1979) Alteration of collagen metabolism in hereditary nephritis. Paediatric Research, 13: 114116.CrossRefGoogle ScholarPubMed
Turner, J. S. (1970) Hereditary hearing loss with nephropathy. Acta Otolaryngologica, Supplement 271.Google ScholarPubMed
West, B. A., Brummell, R. E. and Donna, L. H. (1973) Interaction of Kanamycin and Ethacrynic Acid. Academy of Archives of Otolaryngology, 98: 3237.CrossRefGoogle ScholarPubMed
Weston, T. E. T. (1964) Presbyacusis. Journal of Laryngology and Otology, 78: 272286.CrossRefGoogle ScholarPubMed
Yassin, A., et al. , (1970) The relationship between electrolyte balance and cochlear disturbances in cases of renal failure. Journal of Laryngology and Otology, 84: 429435.CrossRefGoogle ScholarPubMed