Berry-szindróma: Egy ritka komplex veleszületett szívhiba sikeres újszülöttkori korrekciója

Translated title of the contribution: Berry syndrome: Successful neonatal repair for a rare complex malformation

László Környei, László Király, András Szatmári

Research output: Contribution to journalReview article

2 Citations (Scopus)


Aortopulmonary septal defect, interrupted aortic arch, aortic origin of the right pulmonary artery, intact ventricular septum, and patent ductus arteriosus (Berry Syndrome) is a rarely reported malformation. A 6-day-old girl underwent successful one-stage complete repair of direct anastomosis between the ascending and descending aorta, reimplantation of the right pulmonary artery augmented with pericardium patch. Stenosis of the origin of the reimplanted right pulmonary artery was treated by balloon angioplasty at the age of 3 months. The authors emphasise the additive nature of surgical correction and interventional cardiology. Review of the literature reveals this patient to be the 25th reported case with Berry syndrome, and the first of that in Hungary.

Original languageHungarian
Pages (from-to)963-966
Number of pages4
JournalOrvosi hetilap
Issue number18
Publication statusPublished - May 1 2004


ASJC Scopus subject areas

  • Medicine(all)

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