A More Common Mucocutaneous Lesion : Pemphigus

Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/123456789/5004

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DC Field	Value	Language
dc.creator	S.K. Padmakumar	-
dc.creator	S.Sunil	-
dc.date	2011	-
dc.date.accessioned	2013-05-30T12:06:15Z	-
dc.date.available	2013-05-30T12:06:15Z	-
dc.date.issued	2013-05-30	-
dc.identifier	http://a4add.com/remoteupload/uploads/2040/share/13104019731864_myfile.pdf	-
dc.identifier	http://www.doaj.org/doaj?func=openurl&genre=article&issn=09761225&date=2011&volume=2&issue=2&spage=178	-
dc.identifier.uri	http://koha.mediu.edu.my:8181/jspui/handle/123456789/5004	-
dc.description	Pemphigus is a group of potentially life-threatening disease characterized by cutaneous and mucosal blistering. There is a fairly strong genetic background to pemphigus with linkage to HLA class II alleles. Pemphigus vulgaris (PV), the most common and important variant, is an autoimmune blistering disease characterized by circulating pathogenic IgG antibodies against desmoglein 3 and desmoglein 1 autoantibodies. Oral lesions are initially vesiculobullous but readily rupture, new bullae developing as the older ones rupture and ulcerate. Biopsy of perilesional tissue, with histological and immunostaining examinations, is essential to the diagnosis.	-
dc.publisher	Kairali Society of Oral & Maxillofacial Pathologists	-
dc.source	Oral & Maxillofacial Pathology Journal	-
dc.subject	vesiculobullous lesion	-
dc.subject	suprabasal clefting	-
dc.title	A More Common Mucocutaneous Lesion : Pemphigus	-
Appears in Collections:	Health Sciences

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