2015, Number 4
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Rev Cubana Cardiol Cir Cardiovasc 2015; 21 (4)
Not compact ventricular cardiomyopathy. About the diagnosis, complementary examinations and diagnostic errors
Jerez CAM, Echevarría PS, Guevara MG, Aleaga CE, González TA
Language: Spanish
References: 33
Page:
PDF size: 732.47 Kb.
ABSTRACT
The non-compaction cardiomyopathy (MVNC) is a primary genetic entity characterized by abnormalities in the morphology
of the ventricular wall, apparently caused by a disturbance in endomyocardial morphogenesis during embryonic
development, demonstrating the presence and persistence of trabeculations accompanied by recesses intertrabecular
that are perfused from the ventricular cavity, these spaces lacunar intertrabecular have no connection to the coronary
tree. His prognosis is determined by the degree of left ventricular dysfunction, severity of arrhythmias and emerging
occurrence of thromboembolic events, such symptoms that characterize this clinical entity. Validated diagnostic criteria
include the contributions of echocardiogram, magnetic resonance and currently totals computed tomography. There are
heart entities but share some morphological characteristics of myocardial structure, do not meet all the diagnostic criteria
for it.
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