Tricuspid atresia overview: Difference between revisions
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{{CMG}}'''Associate Editor-In-Chief:'''; [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu] [[Priyamvada Singh|Priyamvada Singh, MBBS]] | {{CMG}}'''Associate Editor-In-Chief:'''; [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu] [[Priyamvada Singh|Priyamvada Singh, MBBS]] [mailto:psingh13579@gmail.com]; '''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
==Overview== | ==Overview== | ||
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Revision as of 19:40, 7 January 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor-In-Chief:; Keri Shafer, M.D. [2] Priyamvada Singh, MBBS [3]; Assistant Editor-In-Chief: Kristin Feeney, B.S. [4]
Overview
Tricuspid atresia is a form of congenital heart disease whereby the following defects are seen: complete absence of the tricuspid valve, absence of right atrioventricular connection, hypoplastic or an absence of the right ventricle. For survival of the infant a right-to-left atrial shunt is necessary. Repair of this lesion occurs in the first week of life and involves surgical palliation usually in three stages.