Patent foramen ovale risk factors: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 18: | Line 18: | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Needs content]] | [[Category:Needs content]] | ||
[[Category:Up-To-Date cardiology]] | |||
[[Category:Up-To-Date]] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} |
Revision as of 23:41, 20 January 2013
Patent Foramen Ovale Microchapters |
Diagnosis |
---|
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 |
Please help WikiDoc by more adding more content here. It's easy! Click here to learn about editing.
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.