Cardiac magnetic resonance findings in a case of carnitine deficiency

Texas Heart Institute Journal

Volumn 40, Issue 1, 2013, Pages 104-105

  Ascunce, Rebecca Rudominer ^a,b   Nayar, Ambika C ^a   Phoon, Colin K L ^a   Srichai, Monvadi B ^a,c  

^a NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WEILL CORNELL MEDICAL CENTER   (United States)

^c GEORGETOWN UNIVERSITY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE; GADOLINIUM;

ADULT; CARDIOVASCULAR MAGNETIC RESONANCE; CARNITINE DEFICIENCY; CASE REPORT; CHILD; CONGESTIVE HEART FAILURE; CONTRAST ENHANCEMENT; DYSPNEA; FAMILY HISTORY; FATIGUE; FEMALE; HEART LEFT VENTRICLE FAILURE; HEART LEFT VENTRICLE HYPERTROPHY; HUMAN; IMPLANTABLE CARDIOVERTER DEFIBRILLATOR; NONISCHEMIC CARDIOMYOPATHY; NOTE; PATIENT COMPLIANCE; SCHOOL CHILD; SUDDEN DEATH; TRANSTHORACIC ECHOCARDIOGRAPHY;

ARRHYTHMIAS, CARDIAC; CARDIOMYOPATHIES; CARNITINE; CONTRAST MEDIA; DEATH, SUDDEN, CARDIAC; DEFIBRILLATORS, IMPLANTABLE; DIETARY SUPPLEMENTS; ECHOCARDIOGRAPHY; ELECTRIC COUNTERSHOCK; FEMALE; HUMANS; HYPERAMMONEMIA; MAGNETIC RESONANCE IMAGING; MUSCULAR DISEASES; MYOCARDIUM; PREDICTIVE VALUE OF TESTS; TREATMENT OUTCOME; YOUNG ADULT;

EID: 84877694910     PISSN: 07302347     EISSN: 15266702     Source Type: Journal    
DOI: None     Document Type: Note

References (4)

1. Cano A, Ovaert C, Vianey-Saban C, Chabrol B. Carnitine membrane transporter deficiency: a rare treatable cause of cardiomyopathy and anemia. Pediatr Cardiol 2008;29(1):163-5.
2. Amat di San Filippo C, Taylor MR, Mestroni L, Botto LD, Longo N. Cardiomyopathy and carnitine def iciency. Mol Genet Metab 2008;94(2):162-6.
3. Gilbert-Barness E, Barness LA. Pathogenesis of cardiac conduction disorders in children--genetic and histopathologic aspects. Am J Med Genet A 2006;140(19):1993-2006.
4. Longo N, Amat di San Filippo C, Pasquali M. Disorders of carnitine transport and the carnitine cycle. Am J Med Genet C Semin Med Genet 2006;142C(2):77-85.