Mitochondriopathy: a rare aetiology of restrictive cardiomyopathy.

نویسندگان

  • Christophe Thebault
  • Romain Ollivier
  • Guillaume Leurent
  • Pascale Marcorelles
  • Bernard Langella
  • Erwan Donal
چکیده

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.

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عنوان ژورنال:
  • European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology

دوره 9 6  شماره 

صفحات  -

تاریخ انتشار 2008