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Article

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.

American journal of kidney diseases : the official journal of the National Kidney Foundation - 1 Mar 2005

Guigonis Vincent, Frémeaux-Bacchi Véronique, Giraudier Stéphane, Favier Rémi, Borderie Didier, Massy Ziad, Mougenot Béatrice, Rosenblatt David S, Deschênes Georges

Abstract excerpt

BACKGROUND: cblC disease is a cause of hemolytic uremic syndrome (HUS), which has been primarily described in neonates and infants with severe renal and neurological lesions. PATIENTS: Two sisters aged 6 and 8.5 years presented with a latent hemolytic process characterized by undetectable or low plasma haptoglobin, respectively, associated with renal failure and gross proteinuria. Renal biopsies performed in both...

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PMID: 15754282
DOI: 10.1053/j.ajkd.2004.12.004

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

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