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Hypertrophic cardiomyopathy in childhood.

Colan, SD; (2010) Hypertrophic cardiomyopathy in childhood. Heart Fail Clin , 6 (4) 433-iii. 10.1016/j.hfc.2010.05.004.

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Abstract

Hypertrophic cardiomyopathy has important differences in children compared with adults, particularly with regard to the range of causes and the outcomes in infants. Survival is highly dependent on etiology, particularly in the youngest patients, and pursuit of the specific cause is therefore necessary. The clinical utility of defining the genotype in children with familial hypertrophic cardiomyopathy exceeds that at other ages and has a highly favorable cost/benefit ratio. Although most of the available information concerning treatment and prevention of sudden death is derived in adults, management of children requires consideration of the differences in age-specific risk/benefit ratios.

Type: Article
Title: Hypertrophic cardiomyopathy in childhood.
Location: United States
DOI: 10.1016/j.hfc.2010.05.004
Keywords: Ablation Techniques, Adrenergic beta-Antagonists, Angiotensin-Converting Enzyme Inhibitors, Anti-Arrhythmia Agents, Arrhythmias, Cardiac, Calcium Channel Blockers, Cardiomyopathy, Hypertrophic, Child, Death, Sudden, Defibrillators, Implantable, Ethanol, Exercise, Genetic Predisposition to Disease, Heart Septum, Humans, Magnetic Resonance Imaging, Myocardial Bridging, Myocardium, Pacemaker, Artificial, Severity of Illness Index, Syncope, Ventricular Outflow Obstruction
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science
URI: http://discovery.ucl.ac.uk/id/eprint/1349576
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