ATYPICAL HAEMOLYTIC UREMIC SYNDROME-Reference-Cited by-同舟云学术

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ATYPICAL HAEMOLYTIC UREMIC SYNDROME

Published:2020-12-01 Issue: Volume: Page:38-40
ISSN:
Container-title:INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH
language:en
Short-container-title:ijsr

Author:

R Somasekar¹

Affiliation:

1. Professor, Department of Pediatrics, Sree Balaji Medical College & Hospital, Chennai.

Abstract

This is a case of 7-year-old child who presented with typical characteristics of HUS who developed complications in various systems but responded with timely treatment.

Publisher

World Wide Journals

Reference21 articles.

1. Alejandra Rosales, Magdalena Riedl and Lothar B. Zimmerhackl. Atypical HUS : current diagnostic and therapeutic approaches. Nephrology nature reviews. 2010 volume 6.

2. Blackall DP, Marques MB. Hemolytic uremic syndrome revisited: Shiga toxin, factor H, and fibrin generation. Am J ClinPathol. 2004;121 suppl:S81-8.

3. Burns ER, Lou Y, Pathak A. Morphologic diagnosis of thrombotic thrombocytopenic purpura. Am J Hematol. 2004;75(1):18-21.

4. Caprioli J, Bettinaglio P, Zipfel PF, et al. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. J Am SocNephrol. 2001;12(2):297-307.

5. Davis AK, Makar RS, Stowell CP, Kuter DJ, Dzik WH. ADAMTS13 binds to CD36: a potential mechanism for platelet and endothelial localization of ADAMTS13. Transfusion. 2009;49(2):206-13.

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