Transposition of the great vessels causes: Difference between revisions
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{{Template:Transposition of the great vessels}} | {{Template:Transposition of the great vessels}} | ||
{{CMG}} | {{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh@perfuse.org]; {{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@perfuse.org] | ||
'''Associate | |||
==Overview== | |||
==Causes== | ==Causes== | ||
The cause of most congenital heart defects is unknown. | The cause of most congenital heart defects is unknown. | ||
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*Rubella or other viral illness during pregnancy | *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. | *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. | ||
==References== | ==References== |
Revision as of 13:22, 10 August 2011
Transposition of the great vessels Microchapters |
Classification |
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Differentiating Transposition of the great vessels from other Diseases |
Diagnosis |
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Surgery |
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Transposition of the great vessels causes On the Web |
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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
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.