Total anomalous pulmonary venous connection epidemiology and demographics: Difference between revisions
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{{CMG}} '''Associate Editor-In-Chief:'''{{CZ}}; [[Priyamvada Singh|Priyamvada Singh, MBBS]] [[mailto: | {{CMG}} '''Associate Editor-In-Chief:'''{{CZ}}; [[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== |
Revision as of 18:33, 2 November 2012
Total anomalous pulmonary venous connection Microchapters |
Differentiating Total anomalous pulmonary venous connection from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor-In-Chief:Cafer Zorkun, M.D., Ph.D. [2]; Priyamvada Singh, MBBS [[3]]Assistant Editor-In-Chief: Kristin Feeney, B.S. [[4]]
Overview
Total anomalous pulmonary venous connection is a rare cyanotic congenital heart disease and occurs in 6 to 12 per 100,000 live births.
Incidence[1]
- It's a rare cyanotic congenital heart disease
- 6 to 12 per 100,000 live births.
- It is the fifth most commonest cause of cyanotic heart disease
- Among the congenital heart disease, the incidence of TAPVC ranges between 0.7 - 1.5 percent.
References
- ↑ Reller MD, Strickland MJ, Riehle-Colarusso T, Mahle WT, Correa A (2008). "Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005". J Pediatr. 153 (6): 807–13. doi:10.1016/j.jpeds.2008.05.059. PMC 2613036. PMID 18657826.