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In this study, we present a 3-year-old kid, who was simply identified by chance with congenital AAA at first procedure. We replaced the AAA+coarctation with a 6-mm polytetrafluoroethylene (PTFE) graft. Histological examination of the aortic wall disclosed no certain abnormalities. Collateral vessels were noted to develop over 14 several years of followup. Good blood flow to both lower limbs with no intermittent claudication were observed. After growth, in the age 17, he underwent extra-anatomical b