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A Clinician's Guide to Pemphigus VulgarisAnalysis of Pemphigus Vulgaris

A Clinician's Guide to Pemphigus Vulgaris: Analysis of Pemphigus Vulgaris [There are two main different variants of pemphigus vulgaris: one is the mucocutaneous variant and the other is the mucosal dominant variant. The mucosal dominant variant of pemphigus vulgaris involves autoantibodies against only desmoglein 3, whereas the mucocutaneous variant involves autoantibodies against both desmoglein 1 and 3. Some patients, however, report never having musocal lesions and are classified as having cutaneous-only disease.] http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png

A Clinician's Guide to Pemphigus VulgarisAnalysis of Pemphigus Vulgaris

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References (1)

  • D. Murrell, Sarah Dick, Abdul Ahmed, M. Amagai, M. Barnadas, L. Borradori, J. Bystryn, G. Cianchini, L. Diaz, D. Fivenson, R. Hall, K. Harman, T. Hashimoto, M. Hertl, N. Hunzelmann, P. Iranzo, P. Joly, M. Jonkman, Y. Kitajima, N. Korman, L. Martin, D. Mimouni, A. Pandya, A. Payne, David Rubenstein, H. Shimizu, A. Sinha, D. Sirois, D. Zillikens, V. Werth (2008)

    Consensus statement on definitions of disease, end points, and therapeutic response for pemphigus.

    Journal of the American Academy of Dermatology, 58 6

Publisher
Springer International Publishing
Copyright
© Springer International Publishing AG 2018
ISBN
978-3-319-67758-3
Pages
17 –19
DOI
10.1007/978-3-319-67759-0_5
Publisher site
See Chapter on Publisher Site

Abstract

[There are two main different variants of pemphigus vulgaris: one is the mucocutaneous variant and the other is the mucosal dominant variant. The mucosal dominant variant of pemphigus vulgaris involves autoantibodies against only desmoglein 3, whereas the mucocutaneous variant involves autoantibodies against both desmoglein 1 and 3. Some patients, however, report never having musocal lesions and are classified as having cutaneous-only disease.]

Published: Nov 27, 2017

Keywords: Pemphigus vulgaris; Mucocutaneous variant; Mucosal dominant variant; Desmoglein; Autoantibodies; Musocal lesions; Cutaneous-only disease; Early endpoints; Late endpoints; Relapse; Flare; Treatment failure

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