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Sensorineural hearing loss and the Marinesco-Sjögren syndrome

Published online by Cambridge University Press:  29 June 2007

V. E. Newton
V. E. Newton*
Affiliation:
Manchester
*
Valerie Newton, M.D., MSc, Centre for Audiology, School of Education, The University, Oxford Road, Manchester M13 9PL.
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Abstract

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Sensorineural hearing loss has not been previously reported in patients with the Marinesco-Sjögren Syndrome. Two siblings are described where hearing was initially normal but subsequently deteriorated.

Keywords

Deafness, sensorineuralMarinesco-Sjögren syndrome
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 105 , Issue 3 , March 1991 , pp. 210 - 212
Copyright
Copyright © JLO (1984) Limited 1991

References

Alter, M., Kennedy, W. (1968) The Marinesco-Sjögren Syndrome. Minnesota Medicine, 51: 901–906.Google ScholarPubMed
Alter, M., Talbert, R., Croffead, G. (1962) Cerebellar ataxia, congenital cataracts retarded somatic and mental maturation. Neurology, 13: 836–847.CrossRefGoogle Scholar
Garland, H., Moorhouse, D. (1953) An extremely rare recessive hereditary syndrome including cerebellar ataxia, oligophrenia, cataract and other features. Journal of Neurology, Neurosurgery, and Psychiatry, 16: 110–116.CrossRefGoogle ScholarPubMed
Hakamada, S., Sobue, G., Watanabe, K., Kumagai, T., Hara, K., Miyazaki, S. (1981) Peripheral neuropathy in Marinesco-Sjögren syndrome. Brain and Development, 3: 403–406.CrossRefGoogle ScholarPubMed
Marinesco, G., Drägäsnesco, S. T., Vasiliu, D. O. (1931) Nouvelle maladie familiale caracterisée par une cataracte congenitale et un arrét du developpement somato-neuro-psychique. Encephale, 26: 97–109.Google Scholar
Moravcsik, E. E. (1904) Friedreich'sche hereditaere Ataxie. Orvosi Hetilap. Nr. 22 (in Hungarian); cited by Superneau, et al., 1985.Google Scholar
Nolan, M., McCartney, E., McArthur, K., Rowson, V. J. (1980) A study of the hearing and receptive vocabulary of the trainees of an adult training centre. Journal of Mental Deficiency Research, 24: 271–286.Google ScholarPubMed
Nyberg-Hansen, R., Gronvik, O., Refsum, S. (1972) Hereditary cerebellar ataxia associated with congenital cataracts. Four cases of the Marinesco-Sjögren Syndrome with some unusual features. Acta Neurologic Scandinavica, Supplement S1: 257–260.Google Scholar
Sjögren, T. (1950) Hereditary congenital spino-cerebellar ataxia accompanied by congenital cataracts and oligophrenia. Confinia Neurologica, 10: 293–308.CrossRefGoogle Scholar
Skra, H., Berk, K. (1977) Linkage studies on the Marinesco-Sjögren Syndrome and hypergonadotrophic hypogonadism. Clinical Genetics, 11: 57–66.CrossRefGoogle Scholar
Superneau, D., Wertelecki, W., Zellweger, H. (1985) Letter to the Editor: The Marinesco-Sjögren Syndrome described a quarter of a century before Marinesco. American Journal of Medical Genetics, 22: 647–648.CrossRefGoogle Scholar
Yamanaga, H., Ideta, T., Okajima, T., Monmoto, K., Nagaki, J. (1980) Marinesco-Sjögren Syndrome associated with peripheral nerve involvement. Report of three cases in a family. Clinical Neurology, 20: 326–332.Google ScholarPubMed