Hypertrophic cardiomyopathy complicated by severe bradycardias: A pedigree report

Clinical Cardiology

Volumn 25, Issue 2, 2002, Pages 76-80

  Wang, Dao Wen ^a   Deng, You Bin ^b  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Atrioventricular block; Bradycardia; Hypertrophic cardiomyopathy; Pedigree; Sinus dysfunction; Sudden death

Indexed keywords

ADULT; ARTICLE; ATRIOVENTRICULAR CONDUCTION; DISEASE SEVERITY; ECHOCARDIOGRAPHY; FEMALE; GENE MUTATION; HEART LEFT VENTRICLE HYPERTROPHY; HEART MURMUR; HOLTER MONITORING; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MAJOR CLINICAL STUDY; MALE; RECURRENT DISEASE; SINUS BRADYCARDIA; SYNCOPE; TACHYCARDIA;

EID: 0036157148     PISSN: 01609289     EISSN: None     Source Type: Journal    
DOI: 10.1002/clc.4950250207     Document Type: Article

References (7)

1. Recent advances in the molecular genetics of hypertrophic cardiomyopathy
2. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin protein C gene
3. α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
4. Mutations in the gene for cardiac myosinbinding protein C and late-onset familial hypertrophic cardiomyopathy
5. Hemodynamic and electrophysiologic evaluation of patients with hypertrophic cardiomyopathy surviving cardiac arrest
6. A case of nonobstructive hypertrophic cardiomyopathy associated with ventricular tachycardia and sick sinus syndrome
7. Heart conduction disturbances and cardiovascular collapse after disopyramide and low-dose metoprolol in a patient with hypertrophic obstructive cardiomyopathy