Review
doi: 10.1016/j.jcms.2010.02.006.
Epub 2010 Mar 25.
Xeroderma pigmentosum: a review and case series
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- PMID: 20346687
- DOI: 10.1016/j.jcms.2010.02.006
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Review
Xeroderma pigmentosum: a review and case series
J Craniomaxillofac Surg.
2010 Oct.
Abstract
Xeroderma 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.
Copyright © 2010 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
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