Cardiomyopathy in multiple acyl-CoA dehydrogenase deficiency: A clinico-pathological correlation and review of literature

Pediatric Cardiology

Volumn 29, Issue 2, 2008, Pages 446-451

  Singla, Mohit ^a   Guzman, Grace ^a   Griffin, Andrew J ^a   Bharati, Saroja ^a,b,c  

^a UNIVERSITY OF ILLINOIS   (United States)

^b ADVOCATE CHILDREN S HOSPITAL   (United States)

^c RUSH UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Cardiomyopathy; Glutaric acidemia Type II; Multiple acyl CoA dehydrogenase deficiency

Indexed keywords

ACYL COENZYME A DEHYDROGENASE;

ACYL COENZYME A DEHYDROGENASE DEFICIENCY; ANAMNESIS; ARTICLE; AUTOPSY; CARDIOMYOPATHY; CASE REPORT; CHILD CARE; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; ECHOCARDIOGRAPHY; ENZYME DEFICIENCY; HOSPITAL ADMISSION; HUMAN; INFANT; LABORATORY TEST; MALE; MASS SPECTROMETRY; NEWBORN SCREENING; PERICARDIAL EFFUSION; PHYSICAL EXAMINATION; THORAX RADIOGRAPHY; TRICUSPID VALVE DISEASE;

BIOLOGICAL MARKERS; CARDIOMYOPATHIES; DIAGNOSIS, DIFFERENTIAL; ECHOCARDIOGRAPHY; FATAL OUTCOME; HUMANS; INFANT; MALE; MULTIPLE ACYL COENZYME A DEHYDROGENASE DEFICIENCY; MYOCARDIUM; RADIOGRAPHY, THORACIC;

EID: 40949113699     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00246-007-9119-6     Document Type: Article

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