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Article

Atypical haemolytic uraemic syndrome: a case of rare genetic mutation.

BMJ case reports - 30 Jul 2021

Sangeetha Geminiganesan, Jayaraj Jaippreetha, Ganesan Swathi, Puttagunta Sreeapoorva

Abstract excerpt

Complement-mediated kidney disease has been an evolving area in the field of nephrology. Atypical haemolytic uraemic syndrome (aHUS) is a rare thrombotic microangiopathy that affects multiple organs, particularly kidneys. The disease is characterised by a triad of haemolytic anaemia, thrombocytopenia and acute kidney injury (AKI). aHUS is most commonly caused by dysregulation of alternative complement pathway. In...

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Identifiers

PMID: 34330731
DOI: 10.1136/bcr-2021-244190
PMCID: PMC8327850

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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