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Atypical Hemolytic Uremic Syndrome in a Child: A Rare Case Report

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Journal Clin Case Rep
Date 2024 Jan 1
PMID 38161638
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Abstract

Atypical hemolytic uremic syndrome, a rare thrombotic microangiopathy, necessitates early diagnosis and comprehensive care due to its potential severity, emphasizing the importance of a multidisciplinary approach to improve outcomes.

Citing Articles

Atypical hemolytic uremic syndrome in a child: A rare case report.

Kunwor B, Sharma B, Chhetri S, Joshi P, Pradhan D Clin Case Rep. 2024; 12(1):e8356.

PMID: 38161638 PMC: 10753129. DOI: 10.1002/ccr3.8356.

References
1.
Zimmerhackl L, Besbas N, Jungraithmayr T, van de Kar N, Karch H, Karpman D . Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndrome. Semin Thromb Hemost. 2006; 32(2):113-20. DOI: 10.1055/s-2006-939767. View

2.
Goodship T, Cook H, Fakhouri F, Fervenza F, Fremeaux-Bacchi V, Kavanagh D . Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference. Kidney Int. 2016; 91(3):539-551. DOI: 10.1016/j.kint.2016.10.005. View

3.
Loirat C, Fremeaux-Bacchi V . Atypical hemolytic uremic syndrome. Orphanet J Rare Dis. 2011; 6:60. PMC: 3198674. DOI: 10.1186/1750-1172-6-60. View

4.
Raina R, Krishnappa V, Blaha T, Kann T, Hein W, Burke L . Atypical Hemolytic-Uremic Syndrome: An Update on Pathophysiology, Diagnosis, and Treatment. Ther Apher Dial. 2018; 23(1):4-21. DOI: 10.1111/1744-9987.12763. View

5.
Kaplan B, Meyers K, Schulman S . The pathogenesis and treatment of hemolytic uremic syndrome. J Am Soc Nephrol. 1998; 9(6):1126-33. DOI: 10.1681/ASN.V961126. View