Dilated cardiomyopathy differential diagnosis: Difference between revisions
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|[[Noncompaction cardiomyopathy|Left ventricular noncompaction]] | |[[Noncompaction cardiomyopathy|Left ventricular noncompaction]] | ||
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* Genetic mutations (sporadic or [[familial]]) | |||
* [[Autosomal dominant inheritance|Autosomal-dominant]] inheritance | |||
| | | | ||
| | * D[[Dyspnea on exertion|yspnea on exertion]] | ||
* [[Fatigue]] | |||
* [[Pedal edema]] | |||
* [[Exercise intolerance]] | |||
* In infants, [[cyanosis]], dysmorphic features, and [[failure to thrive]] | |||
|Diagnosis can be based on: | |||
* Echocardiography | |||
* Steady-state free precession MRI, showing prominent trabeculations and a non-compacted to compacted (NC/C) myocardium ratio > 2.3 | |||
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|[[Myocarditis]] | |[[Myocarditis]] |
Revision as of 07:06, 9 December 2019
Dilated cardiomyopathy Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Dilated cardiomyopathy differential diagnosis On the Web |
American Roentgen Ray Society Images of Dilated cardiomyopathy differential diagnosis |
Risk calculators and risk factors for Dilated cardiomyopathy differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdelrahman Ibrahim Abushouk, MD[2]
Overview
Dilated cardiomyopathy should be differentiated from other causes of cardiac dysfunction
Differentiating Beriberi from other Diseases
Dilated cardiomyopathy should be differentiated from other causes of cardiac dysfunction
Disorders | Etiology | Clinical Presentation | Laboratory Findings |
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Acute Coronary Syndrome |
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Acute Pericarditis |
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Amphetamine/Cocaine
Cardiomyopathy |
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Arrhythmogenic right ventricular
cardiomyopathy (ARVC/D) |
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Diagnostic criteria are based on:
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Wet Beriberi |
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Cardiac Tamponade |
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Hyperthyroidism |
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Hypertrophic Cardiomyopathy |
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The diagnosis is based on
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Left ventricular noncompaction |
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Diagnosis can be based on:
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Myocarditis | |||
Restrictive Cardiomyopathy |
References