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Published in: Orphanet Journal of Rare Diseases 1/2019

Open Access 01-12-2019 | Magnetic Resonance Imaging | Letter to the Editor

Left ventricular clefts – incidental finding or pathologic sign of Wilson’s disease?

Authors: Kun Zhang, Ulrike Reuner, Marie Weidauer, Uwe Speiser, Karim Ibrahim, Marian Christoph, Frank R. Heinzel, Burkert Pieske, Felix M. Heidrich, Silvio Quick

Published in: Orphanet Journal of Rare Diseases | Issue 1/2019

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Abstract

Background

Wilson’s disease is an inherited autosomal recessive multi-systemic disorder characterized by reduced excretion and consequently excessive accumulation of copper in different organs, such as the heart.

Results

In a prospective controlled trial, which is the largest to date, we evaluated 61 patients with Wilson’s disease, age- and sex-matched to 61 healthy patients, for cardiac manifestation using cardiac magnetic resonance imaging. Patients were under stable disease and had no signs of heart failure at the time of examination.
We detected a left ventricular cleft, an invagination penetrating more than 50% wall thickness of the adjoining compact myocardium in diastole, in 20% of the patients (12 out of 61) compared to 5% among control patients (3 out of 61, p = 0.013). No correlation between the incidence of cleft and a certain genotype of Wilson’s disease was found. All described cases were incidental findings and none of the patients showed other signs of cardiac involvement.

Conclusions

To conclude, the results of this study suggests that the increased occurrence of left ventricular clefts is due to Wilson’s disease. Large studies with a long observation period are needed for further evaluation.
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Metadata
Title
Left ventricular clefts – incidental finding or pathologic sign of Wilson’s disease?
Authors
Kun Zhang
Ulrike Reuner
Marie Weidauer
Uwe Speiser
Karim Ibrahim
Marian Christoph
Frank R. Heinzel
Burkert Pieske
Felix M. Heidrich
Silvio Quick
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2019
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-019-1238-7

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