Ebstein's anomaly of the tricuspid valve history: Difference between revisions
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{{Congenital malformations and deformations of circulatory system}} | {{Congenital malformations and deformations of circulatory system}} | ||
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[[Category:Cardiology]] | |||
[[Category:Pediatrics]] |
Latest revision as of 17:54, 12 December 2011
Ebsteins anomaly of the tricuspid valve Microchapters | |
Diagnosis | |
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Treatment | |
Case Studies | |
Ebstein's anomaly of the tricuspid valve history On the Web | |
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Ebstein's anomaly of the tricuspid valve history in the news | |
Risk calculators and risk factors for Ebstein's anomaly of the tricuspid valve history | |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] and Claudia P. Hochberg, M.D. [2]
Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [3]
History
- Presentation depends greatly on the degree of apical displacement of the tricuspid valve leaflet as well as the degree of dysfunction of the tricuspid valve. If the tricuspid valve is severely deformed, fetal hydrops may occur. If the valve is functioning, patients may remain symptom free for many years.
- Palpitations may occur secondary to SVTs (supraventricular tachycardia) and WPW (Wolff-Parkinson-White syndrome) (8%).
- Growth and development are normal.
References