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dc.contributor.authorOdhiambo, Andrew O
dc.contributor.authorKaminja, Kenneth
dc.contributor.authorMunyao, Titus
dc.date.accessioned2015-03-25T09:37:40Z
dc.date.available2015-03-25T09:37:40Z
dc.date.issued2015
dc.identifier.citationOdhiambo A.(2015 ). Case report of Xeroderma pigmentosum associated with multiple skin cancers and strong family history.Afr J Haematol Oncol,5:15-18en_US
dc.identifier.urihttp://hdl.handle.net/11295/81669
dc.description.abstractXeroderma pigmentosum (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 a defect in DNA repair. A case of stage 3 Xeroderma pigmentosum affecting a young girl and her siblings is presented. This is a rare medical condition which may cause difficulties in making a timely diagnosis.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.subjectXeroderma Pigmentosum; Squamous Cell Carcinoma; Hyperpigmentation; Photophobia; Sub- Saharan Africa.en_US
dc.titleCase report of Xeroderma pigmentosum associated with multiple skin cancers and strong family history.en_US
dc.typeArticleen_US
dc.type.materialen_USen_US


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