Publication:
Recurrent haemolytic-uraemic syndrome with hypocomplementaemia: a case report

dc.contributor.authorBogdanović, Radovan (7004665744)
dc.contributor.authorČvorić, Angelina (6601985006)
dc.contributor.authorNikolić, Vesna (7102074111)
dc.contributor.authorSindjić, Miodrag (6603973132)
dc.date.accessioned2025-06-12T11:56:25Z
dc.date.available2025-06-12T11:56:25Z
dc.date.issued1988
dc.description.abstractA boy who developed haemolytic-uraemic syndrome (HUS) at 8 years 6 months of age had four further episodes of the disease during the next 3 years. No renal abnormalities were detected between the attacks nor in the 2.5 years after the last recurrence. Reduced levels of serum complement were found during four of the episodes and in two intervening periods. © 1988 IPNA.
dc.identifier.urihttps://doi.org/10.1007/BF00862598
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0023817985&doi=10.1007%2fBF00862598&partnerID=40&md5=f98cfd255bee335bb9a7b956195bcacc
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/1945
dc.subjectHypocomplementaemia
dc.subjectRecurrent haemolytic uraemic syndrome
dc.titleRecurrent haemolytic-uraemic syndrome with hypocomplementaemia: a case report
dspace.entity.typePublication

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