Hostname: page-component-cd9895bd7-dk4vv Total loading time: 0 Render date: 2024-12-29T12:05:28.187Z Has data issue: false hasContentIssue false
  • English
  • Français

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.
Get access Rights & Permissions [Opens in a new window]

Abstract

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

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

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