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Otological disease in Turner's syndrome

Published online by Cambridge University Press:  29 June 2007

P. M. Watkin
P. M. Watkin*
Affiliation:
London
*
Dr Peter M. Watkin, The Hearing Unit, Hurst Rd. Health Centre, Walthamstow, London E17.
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Type
Main Articles
Information
The Journal of Laryngology & Otology , Volume 103 , Issue 8 , August 1989 , pp. 731 - 738
Copyright
Copyright © JLO (1984) Limited 1989

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References

Anderson, H., Filipsson, R., Fluur, E., Koch, B., Lindsten, J. and Wedenberg, E.Hearing impairment in Turner's syndrome. Acta Otolaryngologica. Supplement 247.Google Scholar
Arnold, W., Ganzer, U. and Kleinmann, H. (1977) Sensorineural hearing loss in mucous otitis. Archives of Oto-Rhino-Laryngology 215, 91–93.CrossRefGoogle ScholarPubMed
Bohme, G. and Lieschke, H. J. (1969) Relationship between ear diseases and gonadal dysgenesis with chromosomal anomaly. Deutsche Gesundheitswesen 24, 42.Google Scholar
Engel, E. and Forbes, A. (1965) Cytogenic and clinical findings in 48 patients with congenitally defective or absent ovaries. Medicine 44, 2, 135–164.CrossRefGoogle ScholarPubMed
Feingold, M. and Bossert, W. H. (1974) Normal values for selected physical parameters. Birth Defects, Original Article Series X, 13.Google Scholar
Ferguson-Smith, M. A. (1964) Clinical and cytogenetical studies in female gonadal dysgenesis and their bearing on the cause of Turner's syndrome Cytogenetics, 3, 355–383.CrossRefGoogle ScholarPubMed
Fisch, L. (1981) Syndromes Associated with Hearing Loss. In Beagley, H. A. (Ed.). (1981) Audiology and Audiological Medicine. Oxford University Press. Oxford.Google Scholar
Ford, C. E., Jones, K. W., Polani, P. E., De Almeida, J. C. and Briggs, J. H. (1959) A sex chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet 1, 711.CrossRefGoogle Scholar
Goodman, R. and Gorlin, R. J. (1983) The Malformed Infant and Child. Oxford University Press, Oxford.Google Scholar
Haddad, M. D. and Wilkins, L. (1959) Congenital anomalies associated with gonadal aplasia. Pediatrics 23, 885–902.CrossRefGoogle ScholarPubMed
Hook, E. B. and Hamerton, J. L. (1977) The Frequency of Chromosome Abnormalities Detected in Consecutive Newborn Studies. In Hook, E. B. and Porter, I. H. (Eds.) (1977) Population Cytogenetics. Academic Press, New York.Google Scholar
Lemli, L. and Smith, D. W. (1963) The XO Syndrome. A Study of the Differential Phenotype in 25 Patients. Journal of Pediatrics 63, 577.CrossRefGoogle ScholarPubMed
Masters, M. (1988) Turner's Syndrome Stigmata, Turner's Syndrome Association, Child Growth Foundation, 2 Manfield Avenue, Chiswick, London.Google Scholar
Nadol, J. B. (1980) Pathoembryology of the Middle Ear. In Gorlin, R. J. (Ed.) (1980). Morphogenesis and Malformation of the Ear. Alan R. Liss Inc., New York.Google Scholar
Nolan, M. (1978) Guidance on interpretation of information from a sound level meter. Journal of the British Association of Teachers of the Deaf 2, 169–173.Google Scholar
Palmer, C. G. and Reichmann, A. (1976) Chromosomal and clinical findings in 110 females with Turner's syndrome. Human Genetics 35, 35–49.CrossRefGoogle Scholar
Paparella, M. M., Morizono, T., Le, C. T., Mancini, F., Sipila, P., Choo, Y. B., Liden, G. and Kim, C. S. (1984) Sensorineural hearing loss in otitis media. Annals of Otology, Rhinology and Laryngology.CrossRefGoogle ScholarPubMed
Schinzel, A. (1984) Catalogue of Unbalanced Chromosome Aberrations in Man. De Gruyter, Berlin, New York.Google Scholar
Smith, C. W. (1985) Smith-McGuckin spot. Journal of the Royal Society of Medicine 78, 18–26.CrossRefGoogle ScholarPubMed
Smith, D. W., (1982) Recognizable patterns of human malformation. W. B. Saunders, Philadelphia.Google ScholarPubMed
Stratton, H. J. M. (1965) Gonadal dysgenesis and the ears. Journal of Laryngology and Otology 79, 4, 343.CrossRefGoogle ScholarPubMed
Szemja, Z. (1980) Hearing in children with Turner's syndrome. Endokrynologia Polska 31, 5, 441.Google Scholar
Szpunar, J. and Rybak, M. (1968) Middle ear disease in Turner's syndrome. Archives of Otolaryngology 87, 52–58.Google ScholarPubMed
Tucker, I. and Nolan, M. (1984) Educational Audiology. Croom Helm, London.Google Scholar
Turner, H. H. (1938) A syndrome of infantilism, congential webbed neck, and cubitus valgus. Endocrinology 23, 566–574.CrossRefGoogle Scholar
Valentine, G. H. (1975) The Chromosome Disorders. Wm. Heinemann Ltd., London.Google Scholar
Ventry, I. M., Chaiklin, J. and Boyce, W. (1961) Collapse of the ear canal during audiometry. Archives of Otolaryngology 73, 727.CrossRefGoogle ScholarPubMed
Windle-Taylor, P. C., Buchanan, G. and Michaels, L. (1982) The Mondini Defect in Turner's syndrome. A temporal bone report. Clinical Otolaryngology 7, 75–80.CrossRefGoogle ScholarPubMed