Document Detail


Xeroderma pigmentosum: a review and case series.
MedLine Citation:
PMID:  20346687     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Fawzia M A Butt; Jeremiah R Moshi; Sira Owibingire; Mark L Chindia
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Publication Detail:
Type:  Journal Article; Review     Date:  2010-03-25
Journal Detail:
Title:  Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery     Volume:  38     ISSN:  1878-4119     ISO Abbreviation:  J Craniomaxillofac Surg     Publication Date:  2010 Oct 
Date Detail:
Created Date:  2010-09-13     Completed Date:  2010-12-13     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8704309     Medline TA:  J Craniomaxillofac Surg     Country:  Scotland    
Other Details:
Languages:  eng     Pagination:  534-7     Citation Subset:  D; IM    
Copyright Information:
Copyright © 2010 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
Affiliation:
Department of Human Anatomy, University of Nairobi, Kenya. fawzia_butt@yahoo.co.uk
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Carcinoma, Squamous Cell / etiology
Child
Child, Preschool
Conjunctival Neoplasms / etiology
Female
Granuloma, Pyogenic / etiology
Humans
Lip Neoplasms / etiology
Male
Siblings
Tongue Diseases / etiology
Tongue Neoplasms / etiology
Xeroderma Pigmentosum / complications*,  pathology*
Young Adult

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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