Isolated left ventricular non-compaction: the case for abnormal myocardial development
Isolated ventricular non-compaction is an increasingly commonly diagnosed myocardial disorder characterised by excessive and prominent trabeculation of the morphologically left, and occasionally the right, ventricle. This is associated with high rates of thromboembolism, cardiac failure, and cardiac...
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Veröffentlicht in: | Cardiology in the young 2007-04, Vol.17 (2), p.124-129 |
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description | Isolated ventricular non-compaction is an increasingly commonly diagnosed myocardial disorder characterised by excessive and prominent trabeculation of the morphologically left, and occasionally the right, ventricle. This is associated with high rates of thromboembolism, cardiac failure, and cardiac arrhythmia. Recent improvements in understanding the embryonic processes underlying ventricular formation have led to the hypothesis that ventricular non-compaction is due to a failure of normal ventriculogenesis, leading to abnormal myocardium which may present clinically many years later. Experimental work in animal models provides several candidate transcription factors and signalling molecules that could, in theory, cause ventricular non-compaction if disrupted. |
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This is associated with high rates of thromboembolism, cardiac failure, and cardiac arrhythmia. Recent improvements in understanding the embryonic processes underlying ventricular formation have led to the hypothesis that ventricular non-compaction is due to a failure of normal ventriculogenesis, leading to abnormal myocardium which may present clinically many years later. 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This is associated with high rates of thromboembolism, cardiac failure, and cardiac arrhythmia. Recent improvements in understanding the embryonic processes underlying ventricular formation have led to the hypothesis that ventricular non-compaction is due to a failure of normal ventriculogenesis, leading to abnormal myocardium which may present clinically many years later. Experimental work in animal models provides several candidate transcription factors and signalling molecules that could, in theory, cause ventricular non-compaction if disrupted.</description><subject>Animals</subject><subject>Dystrophin - genetics</subject><subject>Dystrophin - metabolism</subject><subject>Echocardiography</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetics</subject><subject>Genotype & phenotype</subject><subject>Heart</subject><subject>Heart - embryology</subject><subject>Heart Defects, Congenital - diagnosis</subject><subject>Heart Defects, Congenital - genetics</subject><subject>Heart Defects, Congenital - metabolism</subject><subject>Heart Ventricles - abnormalities</subject><subject>Heart Ventricles - diagnostic imaging</subject><subject>Humans</subject><subject>hypertrabeculation</subject><subject>molecular biology</subject><subject>Mutation</subject><subject>Myocardium - pathology</subject><subject>Patients</subject><subject>Phenotype</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>Review Article</subject><subject>Risk Factors</subject><subject>Technological change</subject><subject>transcription factors</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><issn>1047-9511</issn><issn>1467-1107</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kE9P3DAQxa2qqPwpH6CXKuqBW8ATO3HSW4uABa2oqgIHLtbEGUNoEm_tBLHfHq92BRIVpxnN-83T02PsC_BD4KCO_gCXqsoBuOKcZ0p8YDsgC5WuLh_jHuV0pW-z3RAeOAchgH9i26AEVJWqdtjNeXAdjtQkHdkxeaRh9K2ZOvTJ4IbUuH6BZmzd8D0Z7ykxGCixzidYD8732CX90hn0TRvXhh6pc4s-enxmWxa7QPubuceuT0-ujmfp_NfZ-fGPeWokL8eUoLR1g6WFLLMEVW5LaypFpIyJZyGxaEwFucnysjJ1JgU3dS0yJFSIshB77GDtu_Du30Rh1H0bDHUdDuSmoBWXHPJSRfDbG_DBTX6I2XQGEqTMiyxCsIaMdyF4snrh2x79UgPXq8b1f43Hn68b46nuqXn92FQcgXQNtGGkpxcd_V9dKKFyXZz91j9vL4uL29lcQ-TFJgT2tW-bO3qN-n6MZyt5mu8</recordid><startdate>200704</startdate><enddate>200704</enddate><creator>Breckenridge, Ross A.</creator><creator>Anderson, Robert H.</creator><creator>Elliott, Perry M.</creator><general>Cambridge University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200704</creationdate><title>Isolated left ventricular non-compaction: the case for abnormal myocardial development</title><author>Breckenridge, Ross A. ; 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This is associated with high rates of thromboembolism, cardiac failure, and cardiac arrhythmia. Recent improvements in understanding the embryonic processes underlying ventricular formation have led to the hypothesis that ventricular non-compaction is due to a failure of normal ventriculogenesis, leading to abnormal myocardium which may present clinically many years later. Experimental work in animal models provides several candidate transcription factors and signalling molecules that could, in theory, cause ventricular non-compaction if disrupted.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>17319979</pmid><doi>10.1017/S1047951107000273</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Dystrophin - genetics Dystrophin - metabolism Echocardiography Genetic Predisposition to Disease Genetics Genotype & phenotype Heart Heart - embryology Heart Defects, Congenital - diagnosis Heart Defects, Congenital - genetics Heart Defects, Congenital - metabolism Heart Ventricles - abnormalities Heart Ventricles - diagnostic imaging Humans hypertrabeculation molecular biology Mutation Myocardium - pathology Patients Phenotype Proteins - genetics Proteins - metabolism Review Article Risk Factors Technological change transcription factors Transcription Factors - genetics Transcription Factors - metabolism |
title | Isolated left ventricular non-compaction: the case for abnormal myocardial development |
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