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- W2897724285 abstract "The clinical experience with Loeys-Dietz syndrome (LDS) reveals fateful natural history with intracerebral incidents and aortic dissections. A newborn child was referred to our hospital with significantly dilated aortic root and clinical signs of LDS phenotype later genetically confirmed as LDS type I. A therapy with antihypertensive medicines was initiated to postpone the surgery. Despite that, aortic root dilatation progressed to 33 mm (z-score +9.3). To avoid aortic rupture, a valve sparing aortic root replacement was performed at patient age of 8 months. The purpose of this report is to share our dilemmas and experience in the treatment of this child." @default.
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- W2897724285 date "2019-05-01" @default.
- W2897724285 modified "2023-09-27" @default.
- W2897724285 title "Valve-Sparing Aortic Root Replacement in an 8-Month-Old Infant With Loeys-Dietz Syndrome" @default.
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- W2897724285 doi "https://doi.org/10.1016/j.athoracsur.2018.07.094" @default.
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