Cyanotic heart defect classification: Difference between revisions
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Created page with "__NOTOC__ {{Cyanotic heart defect}} {{CMG}}; '''Associate Editor-in-Chief:''' Keri Shafer, M.D. [mailto:kshafer@bidmc.harvard.edu] ==Overview== ==Classif..." |
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__NOTOC__ | __NOTOC__ | ||
{{Cyanotic heart defect}} | {{Cyanotic heart defect}} | ||
{{CMG}}; '''Associate Editor-in-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu] | {{CMG}}; '''Associate Editor-in-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu]; {{KD}} | ||
==Overview== | ==Overview== |
Revision as of 21:56, 18 October 2012
Cyanotic heart defect Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-in-Chief: Keri Shafer, M.D. [2]; Kalsang Dolma, M.B.B.S.[3]
Overview
Classification
Cyanotic heart defects, which account for approximately 25% of all congenital heart disease, include:
- Tetralogy of Fallot (ToF)
- Total anomalous pulmonary venous connection
- Hypoplastic left heart syndrome (HLHS)
- Transposition of the great arteries (d-TGA)
- Truncus arteriosus (Persistent)
- Tricuspid atresia
- Interrupted aortic arch
- Coarctation of aorta
- Tricuspid atresia
- Pulmonary atresia (PA)
- Pulmonary stenosis (advanced)