Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-18T05:49:35.542Z Has data issue: false hasContentIssue false
  • English
  • Français

Hearing loss due to cranio-metaphysial dysplasia

Published online by Cambridge University Press:  29 June 2007

D. W. Morgan ,
C. Aldren  and
T. J. Hoare
D. W. Morgan*
Affiliation:
London
C. Aldren
Affiliation:
London
T. J. Hoare
Affiliation:
London
*
D. W. Morgan, B.Sc, F.R.C.S., The Royal National Throat, Nose and Ear Hospital, Gray's Inn Road, London WC1X 8DA.
Get access Rights & Permissions [Opens in a new window]

Abstract

Craniometaphysial dysplasia is a rare cause of conductive hearing loss. It is a genetic disorder of bone due to decreased osteoclastic activity inthe endosteal and periosteal regions of craniofacial and long bones. The characteristic temporal bone abnormalities are attic fixation, abnormallyshaped ossicles and obliterated foramina ovale. Computerised tomography is helpful in predicting operative findings; surgery should be reserved for those with a severe hearing loss.

Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 104 , Issue 10 , October 1990 , pp. 807 - 808
Copyright
Copyright © JLO (1984) Limited 1990

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

Brookes, G. B, Booth, J. B. (1987) Diseases of the Temporal Bone. In: Scott-Brown's Otolaryngology, 5th edn, Volume 3. The Ear (Booth, J. B., Kerr, A. G. eds) Butterworths: London.Google Scholar
Gorlin, R., Sedano, H.O. (1968), Craniometaphyseal dysostosis and craniodiaphysial dysostosis. Modern Medicine, 36: 154–155.Google Scholar
Kietzer, G. and Paparella, M. (1969) Otolaryngological disorders in craniometaphyseal dysplasia, Laryngoscope, 79: 921–941.CrossRefGoogle ScholarPubMed
Millard, D. R., Maisels, D. O., Baitsone, J. H., Yates, B. (1907) Craniofacial surgery in craniometaphyseal dysplasia. American Journal of Surgery, 113: 615–621.CrossRefGoogle Scholar
Rimoin, D., Woodruff, S. (1969) Craniometaphyseal dysplasia–autosomal dominant inheritance in a large kindred. Birth Defects, 5: 96–104.Google Scholar
Rubin, P. (1964) Dynamic classification of bone dysplasia. Year Book, Chicago, 111: p. 410–420.Google Scholar
Schucknecht, H. F. (1963) Stapedectomy. Transactions of the American Otology Society, 51: 181–200.Google Scholar
Shea, J., Gerbe, R., Ayani, N. (1981) Craniometaphyseal dysplasia: the first successful surgical treatment for associated hearing loss. Laryngoscope, 91: 1369–1374.CrossRefGoogle ScholarPubMed