Levo-transposition of the great arteries causes: Difference between revisions
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{{L-transposition of the great arteries}} | {{L-transposition of the great arteries}} | ||
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto: | {{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com]; {{CZ}}; [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu]; '''Assistant Editor(s)-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
==Overview== | ==Overview== | ||
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==References== | ==References== | ||
{{WH}} | |||
{{WS}} | |||
[[Category: | [[Category:Disease]] | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Congenital heart disease]] | [[Category:Congenital heart disease]] | ||
[[Category:Pediatric]] | |||
Latest revision as of 15:29, 2 November 2012
Levo-transposition of the great arteries Microchapters | |
Differentiating Levo-transposition of the great arteries from other Diseases | |
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Treatment | |
Case Studies | |
Levo-transposition of the great arteries causes On the Web | |
American Roentgen Ray Society Images of Levo-transposition of the great arteries causes | |
Risk calculators and risk factors for Levo-transposition of the great arteries causes | |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2]; Cafer Zorkun, M.D., Ph.D. [3]; Keri Shafer, M.D. [4]; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S. [5]
Overview
The cause of most congenital heart defects is unknown.
Causes
The cause of most congenital heart defects is unknown. Factors in the mother that may increase the risk of this condition include:
- Age over 40
- Alcoholism
- Diabetes
- Prenatal nutrition
- Rubella or other viral illness during pregnancy
- Generally, TGA is not known to be associated with any specific single gene defect, but some studies have shown possible genetic association in some cases of TGA, involving deletions of chromosome 22q11.