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      FcγRIIa Polymorphism in Systemic Lupus erythematosus

      research-article
      Kidney and Blood Pressure Research
      S. Karger AG
      Nephritis, Fc=γRIIa Polymorphism, Allotypes, Systemic lupus erythematosus

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          Abstract

          FcγRIIs are the most widely distributed of the Fcγ receptor family and play an important role in the clearance of immune complexes. Evidence that the FcγRIIa–R131 allotype is less able to process and clear immune complexes effectively suggests that this may be a disease susceptibility factor for systemic lupus erythematosus (SLE). Data from studies published thus far do not agree on the potential role of FcγRIIa polymorphism in the genetics of SLE. Most studies in fact show no evidence for any correlation between polymorphism of FcγRIIa and risk for SLE. However, it remains to be determined whether FcγRIIa polymorphism may play a critical role in certain groups of patients, especially in those of differing ethnic background. Polymorphism of FcγRIIa may also be important in determining disease phenotype, and identification of this influence may have important implications in patient care and in identifying patients for more aggressive therapy.

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          Most cited references2

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          Systemic lupus erythematosus.

          B L Kotzin (1996)
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            Ethnic variation in frequency of an allelic polymorphism of human Fcγ RIIA determined with allele specific oligonucleotide probes

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              Author and article information

              Journal
              KBR
              Kidney Blood Press Res
              10.1159/issn.1420-4096
              Kidney and Blood Pressure Research
              S. Karger AG
              1420-4096
              1423-0143
              2000
              2000
              24 March 2000
              : 23
              : 2
              : 138-142
              Affiliations
              Department of Medicine, University Hospital, Kuala Lumpur, Malaysia
              Article
              25967 Kidney Blood Press Res 2000;23:138–142
              10.1159/000025967
              10765117
              d5fe163e-be17-4ef2-9c3b-df7b6a02ca12
              © 2000 S. Karger AG, Basel

              Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

              History
              Page count
              Tables: 3, References: 17, Pages: 5
              Categories
              Fourth Asian Nephrology Forum

              Cardiovascular Medicine,Nephrology
              Nephritis,Fc=γRIIa Polymorphism,Allotypes,Systemic lupus erythematosus

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