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Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis

Includes abstract.

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Bibliographic Details
Main Author: Uwimpuhwe, Henriette
Other Authors: Heckmann, Jeannine
Format: Thesis
Language:English
Published: Department of Human Biology 2014
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access_status_str Open Access
author Uwimpuhwe, Henriette
author2 Heckmann, Jeannine
author_browse Heckmann, Jeannine
Uwimpuhwe, Henriette
author_facet Heckmann, Jeannine
Uwimpuhwe, Henriette
author_sort Uwimpuhwe, Henriette
collection Thesis
description Includes abstract.
format Thesis
id oai:open.uct.ac.za:11427/3208
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:33:43.673Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Human Biology
publisherStr Department of Human Biology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/3208 Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis Uwimpuhwe, Henriette Heckmann, Jeannine Ballo, Robea Prince, Sharon Medicine Includes abstract. Includes bibliographical references (leaves 73-83). Myasthenia gravis (MG) is an autoimmune disorder in which auto-antibodies directed at the acetylcholine receptors (AChR) of the neuromuscular junction (NMJ) block, alter or destroy their targets. The anti-AChR antibodies cause activation of the classical complement pathway leading to inflammatory injury at the NMJ. Decay Accelerating Factor (DAF), a member of complement regulatory proteins, prevents activation of autologous components of complement pathways. The absence of DAF, in knock-out mouse models, has been shown to significantly increase the susceptibility to experimental autoimmune MG. A previous study showed that a high proportion of South African MG patients of African genetic ancestry develop immunosuppressive therapyresistant extraocular muscle (EOM) dysfunction. We hypothesized that these patients have deficient DAF expression in their EOMs resulting in less protection from complement injury. 2014-07-28T18:15:37Z 2014-07-28T18:15:37Z 2009 Master Thesis Masters MSc http://hdl.handle.net/11427/3208 eng application/pdf Department of Human Biology Faculty of Health Sciences University of Cape Town
spellingShingle Medicine
Uwimpuhwe, Henriette
Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis
thesis_degree_str Master's
title Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis
title_full Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis
title_fullStr Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis
title_full_unstemmed Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis
title_short Molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in Myasthenia Gravis
title_sort molecular analysis of decay accelerating factor as a potential susceptibility factor to developing treatment resistant extraocular muscle involvement in myasthenia gravis
topic Medicine
url http://hdl.handle.net/11427/3208
work_keys_str_mv AT uwimpuhwehenriette molecularanalysisofdecayacceleratingfactorasapotentialsusceptibilityfactortodevelopingtreatmentresistantextraocularmuscleinvolvementinmyastheniagravis