Ebsteins anomaly of the tricuspid valve overview: Difference between revisions
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{{CMG}} | {{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}}}; Claudia P. Hochberg, M.D.; [[Priyamvada Singh|Priyamvada Singh, MBBS]] [mailto:psingh@perfuse.org] | ||
'''Associate Editor-In-Chief:''' {{CZ}}}; | |||
== Overview == | == Overview == |
Revision as of 02:10, 20 October 2012
Ebsteins anomaly of the tricuspid valve Microchapters | |
Diagnosis | |
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Treatment | |
Case Studies | |
Ebsteins anomaly of the tricuspid valve overview On the Web | |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]}; Claudia P. Hochberg, M.D.; Priyamvada Singh, MBBS [3]
Overview
Ebstein's anomaly is a congenital heart defect in which the opening of the tricuspid valve is displaced towards the apex of the right ventricle of the heart (congenital apical displacement of the tricuspid valve that typically causes significant tricuspid regurgitation).
Anatomy
The picture below shows displacement of tricuspid valve towards the apex of right ventricle with subsequent atrialization of a portion of the morphologic right ventricle:
Pathophysiology
The annulus of the valve is in normal position. The valve leaflets however, are to a varying degree attached to the walls and septum of the right ventricle. There is subsequent atrialization of a portion of the morphologic right ventricle (which is then contiguous with the right atrium). This causes the right atrium to be large and the anatomic right ventricle to be small in size. 50% of cases involve an atrial shunt (either a PFO or an ASD).
Risk Factors
Administration of Lithium Carbonate or benzodiazepines during pregnancy is associated with a higher risk of Ebstein's anomaly.