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dc.contributor.authorButt, Fawzia MA
dc.contributor.authorMoshi, Jeremiah R
dc.contributor.authorOwibingire, Sira
dc.contributor.authorChindia, Mark L
dc.date.accessioned2013-06-25T06:32:11Z
dc.date.available2013-06-25T06:32:11Z
dc.date.issued2010-10
dc.identifier.citationJournal of Cranio-Maxillofacial Surgery Volume 38, Issue 7, October 2010, Pages 534–537en
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S1010518210000296
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/39364
dc.identifier.uriwww.ncbi.nlm.nih.gov/pubmed/20346687
dc.description.abstractXeroderma pigmentosa (XP) is a condition inherited as an autosomal recessive trait and is characterized by photosensitivity, pigmentary changes, premature skin ageing and malignant tumour development resulting from the defect in DNA repair. The management of complications of XP, especially orofacial tumours entails an enormous surgical challenge to the clinicians. We present five cases of XP.en
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.subjectxeroderma pigmentosum;squamous cell carcinoma;skin hyperpigmentation;photophobiaen
dc.titleXeroderma pigmentosum: a review and case seriesen
dc.typeArticleen
local.publisherDepartment of Human Anatomy, University of Nairobien
local.publisherDepartment of Oral surgery and Pathology, Muhimbili University of Health and Allied Sciences, Dar-es-salaamen
local.publisherDepartment of Oral Maxillofacial Surgery and Pathology, Faculty of Dental Sciences, University of Nairobien


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