Patent foramen ovale risk factors: Difference between revisions
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==References== | ==References== | ||
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[[Category:Cardiology]] | |||
[[Category:Congenital heart disease]] | |||
[[Category:Pediatrics]] | |||
[[Category:Embryology]] | |||
[[Category:Disease]] | |||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} |
Revision as of 18:24, 11 October 2012
Patent Foramen Ovale Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Patent foramen ovale risk factors On the Web |
American Roentgen Ray Society Images of Patent foramen ovale risk factors |
Risk calculators and risk factors for Patent foramen ovale risk factors |
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
Risk Factors
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.