Patent foramen ovale risk factors: Difference between revisions
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
==See also== | |||
*[[Atrioventricular septal defect]] | |||
*[[Congenital heart disease]] | |||
*[[Atrial septal defect]] | |||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Congenital heart disease]] | |||
[[Category:Pediatrics]] | |||
[[Category:Embryology]] | |||
[[Category:Neurology]] | [[Category:Neurology]] | ||
[[Category: | [[Category:Disease]] | ||
[[Category:Mature chapter]] | |||
[[Category:Overview complete]] | |||
[[Category:Up-To-Date]] | |||
{{WikiDoc Help Menu}} | |||
{{WikiDoc Sources}} |
Revision as of 20:09, 8 September 2011
Patent Foramen Ovale Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Priyamvada Singh, M.B.B.S. [2]; Assistant Editor-In-Chief: Kristin Feeney, B.S. [3]
Overview
Insofar as the disorder has been found to occur with an increased frequency in families, there may be at least in part a genetic component in the development of a patent foramen ovale.