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Eur J Cardiothorac Surg 2001;20:1252-1254
© 2001 Elsevier Science NL
Case report |
a Cardiothoracic Unit, Great Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UK
b Institute of Child Health, University College London, London WC1N 1EH, UK
c Cardiac Centre, Bahrain Defence Force Hospital, Bahrain, Arabian Gulf
Received 7 May 2001; received in revised form 20 August 2001; accepted 26 September 2001.
Corresponding author. Tel.: +44-20-7404-4383; fax: +44-20-7831-4931
e-mail: delevm{at}gosh.nhs.uk
We report a rare case of a 2-year-old boy with Down's syndrome, atrioventricular septal defect and so-called absent pulmonary valve syndrome. Diagnostic imaging also revealed the presence of an anomalous high origin of the right coronary artery from the ascending aorta. Surgical repair was successful.
Key Words: Down's syndrome Trisomy 21 Outflow tract malformation Common atrioventricular junction
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