Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an adult male

International Heart Journal

Volumn 53, Issue 6, 2012, Pages 383-387

  Palecek, Tomas ^a,b   Tesarova, Marketa ^a   Kuchynka, Petr ^a   Dytrych, Vladimir ^a   Elleder, Milan ^c   Hulkova, Helena ^c   Hansikova, Hana ^a   Honzik, Tomas ^a   Zeman, Jiří ^a   Linhart, Ales ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

^b ST ANNE S UNIVERSITY HOSPITAL   (Czech Republic)

^c Charles University in Prague and General University Hospital in Prague   (Czech Republic)

Author keywords

Mitochondrial disease; Short PR interval

Indexed keywords

BRAIN NATRIURETIC PEPTIDE; CITRATE SYNTHASE; CYTOCHROME C OXIDASE; LACTIC ACID; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; TROPONIN I;

ADULT; ARTICLE; BASAL GANGLION HEMORRHAGE; BRAIN ISCHEMIA; CARDIAC IMAGING; CARDIOEMBOLIC STROKE; CASE REPORT; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; DISEASE ASSOCIATION; GENE MUTATION; HEART LEFT VENTRICLE EJECTION FRACTION; HEART LEFT VENTRICLE FILLING; HEART MUSCLE BIOPSY; HEART RIGHT BUNDLE BRANCH BLOCK; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERTROPHIC CARDIOMYOPATHY; MALE; MIDDLE CEREBRAL ARTERY; MOLECULAR PATHOLOGY; MUTATIONAL ANALYSIS; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PATIENT ASSESSMENT; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; PR INTERVAL; PRIORITY JOURNAL; QRS COMPLEX; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINUS RHYTHM; SUBARACHNOID HEMORRHAGE; SYSTOLIC HEART MURMUR; TRANSESOPHAGEAL ECHOCARDIOGRAPHY; TRANSTHORACIC ECHOCARDIOGRAPHY; BIOPSY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; ELECTRON MICROSCOPY; GENETICS; HEART MITOCHONDRION; HEART MUSCLE; PATHOLOGY; POINT MUTATION; ULTRASTRUCTURE;

ADULT; BIOPSY; CARDIOMYOPATHY, HYPERTROPHIC; DNA, MITOCHONDRIAL; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; HUMANS; MAGNETIC RESONANCE IMAGING, CINE; MALE; MICROSCOPY, ELECTRON; MITOCHONDRIA, HEART; MITOCHONDRIAL DISEASES; MYOCARDIUM; POINT MUTATION;

EID: 84873744975     PISSN: 13492365     EISSN: 13493299     Source Type: Journal    
DOI: 10.1536/ihj.53.383     Document Type: Article

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