Ranajit B Naik, Divya Mangal, Ankit Mathur
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Primary tricuspid valve disease related to its congenital malformation is rare. Ebstein’s anamoly is a rare congenital condition affecting the septal and posterior leaflets of the tricuspid valve. Ebstein’s anamoly has a wide spectrum of pathological features. We describe the case of 33 year old female with Ebsteinoid tricuspid valve orifice, severely hypoplastic right ventricle and thrombus in a giant right atrium, with intact interatrial and interventricular septa. The patient was managed surgically with Kays tricuspid annuloplasty and right Bidirectional Glenn anastomosis constituting one and a half ventricular repair with satisfactory outcome.
Naik RB, Mangal D, Mathur A. Journal: Journal of Cardiovascular Medicine and Surgery Publication Date: July–December 2024 Volume/Issue: 10(3-4): 84-88
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| Received | Accepted | Published |
|---|---|---|
| September 24, 2024 | November 13, 2024 | December 29, 2024 |
Monday 22 June 2026, 12:31:09 (IST)
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| Received | September 24, 2024 |
| Accepted | November 13, 2024 |
| Published | December 29, 2024 |
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.