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. 1987 Feb;57(2):181–183. doi: 10.1136/hrt.57.2.181

Dilated cardiomyopathy associated with haemolytic uraemic syndrome.

J Poulton, C M Taylor, J V De Giovanni
PMCID: PMC1277102  PMID: 3814452

Abstract

In two children with the haemolytic uraemic syndrome dilated cardiomyopathy occurred in the absence of hypertension, or fluid or electrolyte disturbance. These cases presented with acute left ventricular failure. Echocardiography showed left ventricular dilatation and reduced contractility. There was also ventricular wall thickening, which persisted. Twelve other children with haemolytic uraemic syndrome had prospective echocardiography. Eleven of them showed no evidence of cardiomyopathy and in one transient dilatation and reduced contractility developed without clinical signs. Dilated cardiomyopathy is a rare but important extrarenal manifestation of the haemolytic uraemic syndrome and is best demonstrated by echocardiography.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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