Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-10T20:35:12.040Z Has data issue: false hasContentIssue false
  • English
  • Français

Histopathological studies of the temporal bones in Hurler's disease [Mucopolysaccharidosis (MPS) IH]

Published online by Cambridge University Press:  29 June 2007

I. Friedmann ,
Elizabeth Spellacy ,
Julie Crow  and
R. W. E. Watts
I. Friedmann*
Affiliation:
The Department of Histopathology, Northwick Park Hospital, Harrow HA1 3UJ, U. K. The House Ear Institute, University of Southern California, Los Angels, U.S.A.
Elizabeth Spellacy
Affiliation:
The Division of Inherited Metabolic Diseases, MRC Clinical Research Centre.
Julie Crow
Affiliation:
The Department of Histopathology, Northwick Park Hospital, Harrow HA1 3UJ, U. K.
R. W. E. Watts
Affiliation:
The Division of Inherited Metabolic Diseases, MRC Clinical Research Centre.
*
Professor I. Friedmann, Northwick Park Hospital, and Clinical Research Centre, Watford Road, Harrow, Middlesex HA1 3UJ
Get access Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Research Article
Information
The Journal of Laryngology & Otology , Volume 99 , Issue 1 , January 1985 , pp. 29 - 42
Copyright
Copyright © JLO (1984) Limited 1985

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

REFERENCES

Crome, I. and Stern, J. (1976) In Greenfield's Neuropathology (Eds. Blackwood, W. and Corsellis, J. A. N.). Arnold, London. Third edition, p. 524.Google Scholar
Crow, J., Gibbs, D. A., Cozens, W., Spellacy, E. and Watts, R. W. E. (1983) Biochemical and histopathological studies on patients with mucopolysaccharidoses, two of whom had been treated by fibroblast transplantation. Journal of Clinical Pathology, 36: 415–430.CrossRefGoogle ScholarPubMed
De Lange, C., Gerlings, P. G., De Kleyn, A. and Lettinga, T. W. (1943/1944) Some remarks on gargoylism. Acta Paediatrica (Uppsala), 31: 398–416.CrossRefGoogle Scholar
Friedmann, I. (1974) The Pathology of the Ear. Blackwell, Oxford.Google Scholar
Gerlings, P. G. and De Kleyn, A. (1946) Some remarks about gargoylism (Typus E). Proceedings of the Royal Netherland Academy of Sciences, 49: 29–38.Google Scholar
Gibbs, D. A., Spellacy, E. and Watts, R. W. E. (1980) The treatment of lysosomal storage diseases by fibroblast transplantation: some preliminary observations. Birth Defects, 16: 457–474.Google ScholarPubMed
Gibbs, D. A., Spellacy, E., Tompkins, R., Watts, R. W. E. and Mowbray, J. F. (1983) A clinical trial of fibroblast transplantation for the treatment of mucopolysaccharidoses. Journal of Inherited Metabolic Disease, 6: 62–81.CrossRefGoogle ScholarPubMed
Hurler, G. (1919) Uber einen typ multipler Abartungen, verwiegend am Skelett-system. Zeitschrift für Kinderheilkunde, 24: 220–234.CrossRefGoogle Scholar
Kelemen, G. (1966) Hurler's syndrome and the hearing organ. Journal of Laryngology and Otology, 80: 791–803.CrossRefGoogle ScholarPubMed
Kittel, G. (1963) Pfaundler-Hurler disease or gargoylism from the otorhinolaryngological aspect. Zeitschrift für Laryngologie, Rhinologie und Otologie 42: 206–217.Google ScholarPubMed
Spellacy, E., Kennerley, Bankes J. L., Crow, J., Dourmashkin, R., Shah, D. and Watts, R. W. E. (1980) Glaucoma in a case of Hurler disease. British Journal of Ophthalmology, 64: 773–778.CrossRefGoogle Scholar
Watts, R. W. E., Spellacy, E., Kendall, B. E., du Boulay, G. and Gibbs, D. A. (1981) Computed tomography studies on patients with mucopolysaccharidoses. Neuroradiology, 21: 9–23.CrossRefGoogle ScholarPubMed
Wolff, D. (1942) Microscopic study of temporal bones in dysostosis multiplex (gargoylism). Laryngoscope, 52: 218–223.CrossRefGoogle Scholar