Dyskeratosis congenita in two male cousins

Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/46591

DC Field	Value
dc.title	Dyskeratosis congenita in two male cousins
dc.contributor.author	Loh, H.S.
dc.contributor.author	Koh, M.L.
dc.contributor.author	Giamj, Y.C.
dc.date.accessioned	2013-10-16T05:19:29Z
dc.date.available	2013-10-16T05:19:29Z
dc.date.issued	1987
dc.identifier.citation	Loh, H.S.,Koh, M.L.,Giamj, Y.C. (1987). Dyskeratosis congenita in two male cousins. British Journal of Oral and Maxillofacial Surgery 25 (6) : 492-499. ScholarBank@NUS Repository.
dc.identifier.issn	02664356
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/46591
dc.description.abstract	Dyskeratosis congenita is reported in two male Singaporean Chinese cousins. The family pedigree is presented. Lichen planus or lichenoid lesions, instead of leukoplakia, was the manifestation in the oral cavity. The mode of inheritance and the differential diagnosis of Fanconi's anaemia are discussed. Dental findings are emphasised as such information is lacking in previously reported cases. One of the subjects expired of aplastic anaemia, which together with oral malignancy, is one fatal complication of this disease. © 1987.
dc.source	Scopus
dc.type	Article
dc.contributor.department	ORAL AND MAXILLOFACIAL SURGERY
dc.description.sourcetitle	British Journal of Oral and Maxillofacial Surgery
dc.description.volume	25
dc.description.issue	6
dc.description.page	492-499
dc.description.coden	BJOSE
dc.identifier.isiut	NOT_IN_WOS
Appears in Collections:	Staff Publications

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