Patent foramen ovale risk factors: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Patent foramen ovale}} | {{Patent foramen ovale}} | ||
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{{CMG}}; '''Associate Editors-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com]; '''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | {{CMG}}; '''Associate Editors-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com]; '''Assistant Editor-In-Chief:''' [[Kristin Feeney|Kristin Feeney, B.S.]] [mailto:kfeeney@elon.edu] | ||
==Overview== | ==Overview== |
Revision as of 17:50, 4 January 2013
Patent Foramen Ovale Microchapters |
Diagnosis |
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Treatment |
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Patent foramen ovale risk factors On the Web |
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Risk calculators and risk factors for Patent foramen ovale risk factors |
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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
As the disease occurs with an increased frequency in families, there may be at least in part a genetic component in the development of a patent foramen ovale.