Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-23T08:59:52.705Z Has data issue: false hasContentIssue false

Inherited degenerative chondropathy – an autosomal dominant new clinical entity: report two cases and follow-up of four cases

Published online by Cambridge University Press:  29 June 2007

Mary Kurien*
Affiliation:
Departments of Otolaryngology, Christian Medical College Hospital, Vellore, South India.
M. S. Seshadri
Affiliation:
Departments of General Medicine, Christian Medical College Hospital, Vellore, South India.
Anand Zachariah
Affiliation:
Departments of General Medicine, Christian Medical College Hospital, Vellore, South India.
*
Address for correspondence: Dr Mary Kurien, M.B.B.S., D.L.O., M.S., Associate Professor, Department of ENT, Christian Medical College Hospital,Vellore, Tamil Nadu 632004, South India.

Abstract

Four cases of the rare disorder, inherited degenerative chondropathy have been previously reported (Kurien et al., 1989). A five-year follow-up of these patients and two additional cases are presented in this report. The progress of this disease appears to be arrested after regulardapsone therapy and there was no other organ involvement noted during the follow-up period.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 1995

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

Bauby, F, Suc, B., Vix, J.. Rostykus, P.. Dumas, B.. Douet, F., (1991) Les manifestations ORL de Iapolychrondritc chronique atrophiaute. A propos d'une observation. Annals D Otolarvngologie et de Chiritrgie Cervico-Faciale. 108(1): 6062.Google Scholar
Cyril, M. G., Joseph, P. L. III, (1993) Tracheobronchial and eosphageal manifestations of systemic diseases. In Oiolaryngology-Head and Neck Surgery. 2nd Edition. (Charles, W. C., John, M. F., Lee, A. H., Charles, J. K., David, F. S., eds.). ch. 125. Mosby Year Book. Inc.. St Louis. pp 23002301.Google Scholar
Gouet, D.. Marechud, R.. Neau, J. P.. Abadie, J. C.. Rossi, F.Sudre, Y. (1984) Polychondrite chronique atrophiante. Analyse critique de l'efficacite therapeutique de Ia dapsone: Deux observations. Presse Medicale 13: 723726.Google Scholar
Kurien, M., Seshadri, M. S., Raman, R.. Sen Bhanu, T. (1989) Inherited nasal and laryngeal degenerative chrondropathy. Archives of Otolaryngologv, Head and Neck Sitrgery 115: 746748.CrossRefGoogle Scholar
McAdam, L. P., O'Hanlan, M. A., Bluestone, R.. Pearson, C. M. (1976) Relapsing polychondritis: prospective study of 23 patients and review of literature. Medicine 55: 193215.CrossRefGoogle Scholar
McKusick, V. A. (1966) Heritable Disorders of Connective Tissue, 3rd Edition, Ch. 10, C. V. Mosby Co., St Louis, pp 400480.Google Scholar
Moloney, J. R. (1978) Relapsing polychondritis: its otolaryngological manifestations Journalof Laryngology and Otology 92: 915.CrossRefGoogle ScholarPubMed