Clinical implications of isolated double aortic arch and its complex with intracardiac anomalies

International Journal of Cardiology

Volumn 63, Issue 3, 1998, Pages 205-210

  Lee, Meng Luen ^a   Wang, Jou Kou ^c   Wu, Mei Hwan ^c   Lue, Hung Chi ^c   Ing Sh Chiu, ^b   Chang, Chung I ^b  

^a CHANGHUA CHRISTIAN HOSPITAL   (Taiwan)

^b NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^c NONE

Author keywords

Absent pulmonary valve syndrome; Bicuspid pulmonary valve; DiGeorge syndrome; Double aortic arch; Tetralogy of Fallot; Tricuspid atresia; Ventricular septal defect

Indexed keywords

AORTA ARCH ANOMALY; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; CYANOSIS; DIGEORGE SYNDROME; ECHOCARDIOGRAPHY; ESOPHAGOGRAPHY; FALLOT TETRALOGY; FEEDING DISORDER; FEMALE; HEART FAILURE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; MALE; NEWBORN; PRIORITY JOURNAL; PULMONARY VALVE STENOSIS; RESPIRATORY DISTRESS; TRICUSPID VALVE ATRESIA; WHEEZING;

AORTA, THORACIC; CHILD; CHILD, PRESCHOOL; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; TETRALOGY OF FALLOT; TREATMENT OUTCOME;

EID: 0032574240     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0167-5273(97)00325-2     Document Type: Article

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