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2,033 Possible Causes for No Hypertrophic Cardiomyopathy

  • Cardiomyopathy

    Other Names for Hypertrophic Cardiomyopathy Asymmetric septal hypertrophy Familial hypertrophic cardiomyopathy Hypertrophic nonobstructive cardiomyopathy Hypertrophic obstructive[] Cardiomyopathy - hypertrophic (HCM); IHSS; Idiopathic hypertrophic subaortic stenosis; Asymmetric septal hypertrophy; ASH; HOCM; Hypertrophic obstructive cardiomyopathy Maron[] Practice Essentials Hypertrophic cardiomyopathy (HCM) is a genetic cardiovascular disease.[]

  • Hypertrophic Cardiomyopathy

    What is hypertrophic cardiomyopathy?[] Hypertrophic cardiomyopathy. Prog Cardiovasc Dis. 1994;36:275-308. Google Scholar 11. Marian AJ, Roberts R.[] Codd MB, Sugrue DD, Gersh BJ, Melton LJ: Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy.[]

  • Hypertensive Heart Disease

    Echocardiographic differentiation of hypertensive heart disease and hypertrophic cardiomyopathy.[] OBJECTIVES: European guidelines state left ventricular (LV) end-diastolic wall thickness (EDWT) 15mm suggests hypertrophic cardiomyopathy (HCM), but distinguishing from hypertensive[] cardiomyopathy (HC) from hypertensive heart disease (HHD) and aortic stenosis (AS).[]

  • Syncope

    LVOT gradient may develop not only in hypertrophic cardiomyopathy but also in various heart diseases.[] Syncope in Other Forms of Structural Heart Disease Hypertrophic Cardiomyopathy Hypertrophic cardiomyopathy is a relatively frequent (1 in 500 individuals), genetically determined[] Participation in competitive sports is not recommended for athletes with syncope and phenotype-positive hypertrophic cardiomyopathy, CPVT, LQTS1, or arrhythmogenic right ventricular[]

  • Nonsustained Ventricular Tachycardia

    We present a 40-year-old male with history of nonobstructive hypertrophic cardiomyopathy who presented with lightheadedness.[] Mechanical dispersion by speckle tracking echocardiography is associated with NSVT on 24-h ambulatory ECG monitoring in patients with hypertrophic cardiomyopathy.[] Episodes of NSVT in untreated patients with hypertrophic cardiomyopathy were more frequent during the nighttime.[]

  • Sudden Cardiac Death

    Abstract Hypertrophic cardiomyopathy (HCM) is a heart disease characterized by hypertrophy of the left ventricular myocardium and is most often caused by mutations in sarcomere[] Abstract In search of improved risk stratification in hypertrophic cardiomyopathy (HCM), CMR imaging has been implicated as a potential tool for prediction of sudden cardiac[] cardiomyopathy (HCM), since the first implantable cardioverter defibrillator (ICD) was placed in a human, more than 25 years ago to prevent sudden cardiac death (SCD).[]

  • Dilated Cardiomyopathy

    Dilated cardiomyopathy and hypertrophic cardiomyopathy arise from mutations in many genes.[] Nutritional hypocalcaemic rickets and infantile-onset Pompe disease must always be kept in mind among the causes of concomitant dilated cardiomyopathy and hypertrophic cardiomyopathy[] In addition, each subject with hypertrophic cardiomyopathy who had a TTN variant also had a pathogenic mutation in an established hypertrophic cardiomyopathy gene, suggesting[]

  • Primary Cardiomyopathy

    This type of cardiomyopathy is frequently associated with idiopathic hypertrophic subaortic stenosis.[] Abstract Eleven patients with hypertrophic obstructive cardiomyopathy and eight patients with idiopathic congestive cardiomyopathy underwent extensive neuromuscular studies[] : (1) congestive or dilated cardiomyopathy, (2) hypertrophic cardiomyopathy, and (3) restrictive cardiomyopathy.[]

  • Fabry Disease

    KEYWORDS: Fabry disease; cardiomyopathy, hypertrophic; gadolinium; magnetic resonance; mutation; phenotype; stroke[] Fabry disease continues to be an important misdiagnosis of hypertrophic cardiomyopathy in a clinical setting.[] cardiomyopathy (HCM) and evaluate the diagnostic value of native T1 values beyond age, sex, and conventional imaging features.[]

  • Restrictive Cardiomyopathy

    Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype. Cardiogenetics , 2 (1), e10.[] […] in the presence of the same TNNC1 genotype, prenatally diagnosed hypertrophic cardiomyopathy which evolved into restrictive cardiomyopathy, heart failure and death at the[] […] with hypertrophic cardiomyopathy in affected families.[]

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