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Partial anodontia in a case of Waardenburg's syndrome

Published online by Cambridge University Press:  29 June 2007

Sekhar Bandyopadhyay*
Affiliation:
Department of Otolaryngology, Raiganj Hospital, Raiganj, India
Sheokumar Prasad
Affiliation:
Department of Otolaryngology, Patna Medical College and Hospital, Bihar, India
Pradeep Kumar Singhania
Affiliation:
Department of Otolaryngology, Patna Medical College and Hospital, Bihar, India
*
Address for correspondence: Dr Sekhar Bandyopadhyay, Ukilpara, P.O. Raiganj, Dist – Uttar Dinajpur, West Bengal, IndiaPin – 733 134

Abstract

On routine examination of a case of Waardenburg's syndrome apart from the usual features of the disorder, partial anodontia involving both the lower lateral incisors was evident.

The interesting association of partial anodontia and Waardenburg's syndrome is discussed along with relevant available literature.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 1999

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References

Book, J. A. (1950) Clinical and genetical studies of hypodontia, I premolar aplasia, hyperhidrosis and canities prematura. A new hereditary syndrome in man. American Journal of Human Genetics 2: 240263.Google ScholarPubMed
Fisch, L. (1959) Deafness as part of an hereditary syndrome. Journal of Laryngology and Otology 73: 355381.CrossRefGoogle ScholarPubMed
Foster, S. C., Album, M. M. (1970) Incontinentia pigmenti: Block-Sulzberger, Block-Seimens disease. Oral Surgery 29: 835837.Google Scholar
Friedmann, I. (1974) Pathology of the Ear. 1st Edition. Blackwell Scientific Publications, Oxford, London, Edinburgh, Melbourne, pp 361362.Google Scholar
Gorlin, R. J., Anderson, J. A. (1960) The characteristic dentition of incontinentia pigmenti. Journal of Pediatrics 57: 7885.CrossRefGoogle ScholarPubMed
Levin, L. S., Jorgenson, R. J., Cook, R. A. (1975) Otodental dysplasia: a new ectodermal dysplasia. Clinical Genetics 8: 136144.CrossRefGoogle ScholarPubMed
Pindborg, J. J. (1970) Pathology of the Dental Hard Tissues. Munksgaard, Cophenhagen, p. 23. Quoting from Book, J. A. (1950) American Journal of Human Genetics 2: 240–263.Google Scholar
Redpath, T. H., Winter, G. S. (1969) Autosomal dominant ectodermal dysplasia with significant dental defects. Dental Journal 126: 123128.Google ScholarPubMed
Russell, D. L., Finn, S. B. (1967) Incontinentia pigmenti (Block-Sulzberger Syndrome): a case report with emphasis on dental manifestations. Journal of Dentistry for Children 34: 494500.Google Scholar