Clinical profile and outcome of idiopathic restrictive cardiomyopathy.

@article{Ammash2000ClinicalPA,
  title={Clinical profile and outcome of idiopathic restrictive cardiomyopathy.},
  author={Naser M. Ammash and James B. Seward and Kent R. Bailey and William D. Edwards and A Jamil Tajik},
  journal={Circulation},
  year={2000},
  volume={101 21},
  pages={
          2490-6
        }
}
BACKGROUND Idiopathic restrictive cardiomyopathy is a poorly recognized entity of unknown cause characterized by nondilated, nonhypertrophied ventricles with diastolic dysfunction resulting in dilated atria and variable systolic function. METHODS AND RESULTS Between 1979 and 1996, 94 patients (61% women) 10 to 90 years old (mean, 64 years) met strict morphological echocardiographic criteria for idiopathic restrictive cardiomyopathy, mainly dilated atria with nonhypertrophied, nondilated… CONTINUE READING

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