Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-28T09:40:05.463Z Has data issue: false hasContentIssue false

Dyskeratosis congenita and nasopharyngeal atresia

Published online by Cambridge University Press:  29 June 2007

D. Morrison*
Affiliation:
Department of Respiratory Medicine, City Hospital, Edinburgh.
E. L. Rose
Affiliation:
Department of Respiratory Medicine, Llandough Hospital, Penarth.
A. P. Smith
Affiliation:
Department of Respiratory Medicine, Llandough Hospital, Penarth.
T. H. J. Lesser
Affiliation:
Department of Otolaryngology/Head and Neck Surgery, Walton Hospital, Liverpool.
*
Department of Respiratory Medicine, City Hospital, Greenbank Drive, Edinburgh EH10 5SB

Abstract

Dyskeratosis congenita is a multisystem disorder with an increased incidence of neoplasia and opportunistic infections. A case is reported as a cause of complete nasopharyngeal atresia.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 1992

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

Bennhoff, D. F. (1979) Current management of nasopharyngeal stenosis: indications for Z-plasty. Laryngoscope, 89: 15851592.CrossRefGoogle ScholarPubMed
Cannell, H. (1971) Dyskeratosis congenita. British Journal of Oral Surgery, 9: 820.CrossRefGoogle ScholarPubMed
Cole, H. N., Cole, H. N. Jr., Lascheid, W. P. (1957) Dyskeratosis congenita. Archives of Dermatology, 76: 712719.CrossRefGoogle ScholarPubMed
Connor, J. M., Gatherer, D., Gray, F. C., Pirrit, L. A., Affara, N. A. (1986) Assignment of the gene for dyskeratosis congenita to Xq 28. Human genetics, 72: 348351.CrossRefGoogle Scholar
Connor, J. M., Teague, R. H. (1981) Dyskeratosis congenita. Report of alargekindred. British Journal of Dermatology, 105: 321325.CrossRefGoogle Scholar
Ogden, G. R., Connor, E., Chisholm, D. M. (1988) Dyskeratosis congenita: report of a case and review of the literature. Oral Surgery, Oral Medicine, Oral Pathology, 65: 586591.CrossRefGoogle ScholarPubMed
Sirinavin, C., Trowbridge, A. A. (1975) Dyskeratosis congenita: clinical features and genetic aspects. Journal of Medical Genetics, 12: 339354.CrossRefGoogle ScholarPubMed
Trowbridge, A. A., Sirinavin, C., Linman, J. W. (1977) Dyskeratosis congenita: hematologic evaluation of a sibship and review of the literature. American Journal of Haematology, 3: 143152.CrossRefGoogle ScholarPubMed
Zinsser, F. (1910) Atrophia cutis reticularis cum pigmentatione, dystrophia unguim et leukoplakia oris. Ikonographia Dermatologica, 5: 219223.Google Scholar