Pathologic features of dilated cardiomyopathy with localized noncompaction in a child with deletion 1p36 syndrome

Congenital Heart Disease

Volumn 7, Issue 1, 2012, Pages 59-61

  Pearce, F Bennett ^a   Litovsky, Silvio H ^a   Dabal, Robert J ^a   Robin, Nathaniel ^a   Dure, Leon J ^a   George, James F ^a   Kirklin, James K ^a  

^a UNIVERSITY OF ALABAMA SCHOOL OF MEDICINE   (United States)

Author keywords

Deletion 1p36; Dilated cardiomyopathy; Noncompaction

Indexed keywords

4 HYDROXYPHENYLACETIC ACID; ACYLCARNITINE; INOTROPIC AGENT;

ANTERIOR FONTANEL; ARTICLE; BRACHYCEPHALY; CASE REPORT; CHROMOSOME 1; CHROMOSOME DELETION; CHROMOSOME DELETION 1P36 SYNDROME; COMPARATIVE GENOMIC HYBRIDIZATION; CONGESTIVE CARDIOMYOPATHY; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; ENDOCARDIAL FIBROELASTOSIS; EXTUBATION; EYE MALFORMATION; FACE DYSMORPHIA; FEMALE; GENETIC ANALYSIS; HEART ATRIUM ENLARGEMENT; HEART HYPERTROPHY; HEART LEFT VENTRICLE CONTRACTION; HEART MUSCLE CELL; HEART MUSCLE FIBROSIS; HEART TRANSPLANTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; INTUBATION; KARYOTYPE 46,XX; LIVER CONGESTION; MICROARRAY ANALYSIS; MIDFACE HYPOPLASIA; PERFUSION; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SHOCK; SINUS TACHYCARDIA; SUNKEN EYE; SYSTOLIC DYSFUNCTION; TACHYPNEA; URINALYSIS; VENTRICULAR NONCOMPACTION;

CARDIOMYOPATHY, DILATED; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEART TRANSPLANTATION; HUMANS; INFANT; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; PHENOTYPE;

EID: 84856342763     PISSN: 1747079X     EISSN: 17470803     Source Type: Journal    
DOI: 10.1111/j.1747-0803.2011.00514.x     Document Type: Article

References (7)

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