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Article

Atypical haemolytic uraemic syndrome and mutations in complement regulator genes.

Springer seminars in immunopathology - 1 Nov 2005

Dragon-Durey Marie-Agnès, Frémeaux-Bacchi Véronique

Abstract excerpt

Haemolytic uraemic syndrome (HUS) is a thrombotic microangiopathy (TMA) disorder characterised by the association of haemolytic anaemia, thrombocytopenia and acute renal failure. Atypical forms (non-related to shigatoxin) may be familial or sporadic, with frequent recurrences and most of them lead to end stage renal failure. During the last years, different groups have demonstrated genetic predisposition of...

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Identifiers

PMID: 16189652
DOI: 10.1007/s00281-005-0003-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Atypical haemolytic uraemic syndrome and mutations in complement regulator genes.PMID 16189652Read ↗

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