Mitochondriopathy: A rare aetiology of restrictive cardiomyopathy

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Abstract

When diagnosing a restrictive hypertrophied cardiomyopathy, most echocardiographists consider cardiac amyloidosis as a possible cause, especially after the appearance of 'granular' sparkling echoes on a transthoracic echocardiography. However, other infiltrative diseases (i.e. metabolic myopathies, Gaucher, Hunter's, and Hurler's diseases) or storage cardiomyopathies (haemochromatosis, Fabry's disease, glycogen storage, and Niemann-Pick disease) should be considered. In this paper, we report on another unusual cause of restrictive cardiomyopathy of which all cardiologists should be aware. © The Author 2008.

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APA

Thebault, C., Ollivier, R., Leurent, G., Marcorelles, P., Langella, B., & Donal, E. (2008). Mitochondriopathy: A rare aetiology of restrictive cardiomyopathy. European Journal of Echocardiography, 9(6), 840–845. https://doi.org/10.1093/ejechocard/jen189

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