313 results
diagnosis cardiology differential clinical causes echocardiogram pocus algorithm management takotsubo pathophysiology hypertrophic hocm syndrome table pharmacology a4c treatment signs peds
Primary and Secondary Causes of Cardiomyopathy (a) Primary cardiomyopathies - Genetic - Mixed (genetic/acquired)
Secondary Causes of Cardiomyopathy ... cardiomyopathies - Genetic ... - Mixed (genetic ... Primary #Secondary #Cardiomyopathy
Congestive Heart Failure - Causes, Pathophysiology and Differential Diagnosis • Dilated Cardiomyopathy • Hypertrophic Cardiomyopathy
Diagnosis • Dilated Cardiomyopathy ... • Hypertrophic Cardiomyopathy ... • Restrictive Cardiomyopathy ... Infiltrative • Genetic
Etiologies of hypertrophic cardiomyopathy - Genetic - Storage diseases - Neuromuscular and mitochondrial disorders
of hypertrophic cardiomyopathy ... - Genetic ... #hypertrophic #cardiomyopathy
Etiologies of dilated cardiomyopathy. HF, heart failure; HFrEF, heart failure with reduced ejection fraction; HIV, human
Etiologies of dilated cardiomyopathy ... - Genetic ... Peripartum #dilated #cardiomyopathy
Causes of Dilated Cardiomyopathy DCMP - Differential Diagnosis Algorithm Idiopathic DCMP: Viral, Inflammatory cardiomyopathy, Genetic causes, Unknown
Causes of Dilated Cardiomyopathy ... , Inflammatory cardiomyopathy ... , Genetic causes ... arteritis #Dilated #Cardiomyopathy
Harlequin Ichthyosis Rare genetic disorder that results in thickened skin over nearly the entire surface of the
Ichthyosis Rare genetic ... physicalexam #pediatrics #genetics
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 Hypertrophic Cardiomyopathy (HOCM) - Diagnosis and Management Diagnosis 1. Wall thickness 215 mm (TTE/CT/MRI) 2. Absence
Hypertrophic Cardiomyopathy ... LVH (Supportive: genetic ... #Hypertrophic #Cardiomyopathy
Metabolism of plasma lipoproteins and related genetic diseases - Familial Hypercholesterolemia Type I (FAMILIAL HYPERCHYLOMICRONEMIA) Type IIA
lipoproteins and related genetic ... #lipoproteins #genetics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics
Hypertrophic, Dilated and Arrhythmogenic Cardiomyopathy - Comparison #Hypertrophic #Dilated #Arrhythmogenic #Cardiomyopathy #Comparison #Diagnosis #Management #Cardiomyopathies #Cardiology
Arrhythmogenic Cardiomyopathy ... Arrhythmogenic #Cardiomyopathy
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