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      Charcot-Marie-Tooth Disease and Nephropathy in a Mother and Daughter with a Review of the Literature

      case-report

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          Abstract

          We report a mother-and-child combination of Charcot-Marie-Tooth disease and nephropathy. The mother received a cadaveric renal transplant, and the daughter has heavy proteinuria with normal glomerular filtration rate. There have been 7 single case reports of both disease entities and 1 report of 3 patients which includes the only sib pair. The related literature is reviewed.

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          Author and article information

          Journal
          NEF
          Nephron
          10.1159/issn.1660-8151
          Nephron
          S. Karger AG
          1660-8151
          2235-3186
          1990
          1990
          10 December 2008
          : 54
          : 1
          : 80-85
          Affiliations
          Departments of Medicine and Pathology, Memorial University of Newfoundland, St. John’s, N.F., Canada
          Article
          185814 Nephron 1990;54:80–85
          10.1159/000185814
          2404215
          9d652a9d-3dfb-4e2d-8517-71de2ce7ab22
          © 1990 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
          : 05 May 1989
          Page count
          Pages: 6
          Categories
          Case Report

          Cardiovascular Medicine,Nephrology
          Glomerular basement membrane,Charcot-Marie-Tooth disease,Focal segmental proliferative glomerulonephritis,Renal failure,Hereditary nephritis

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