Journals / Marmara Medical Journal / 2000 / Cilt: 13 - Sayı: 4

Cor triatriatum associated with Ebstein malformation of atretic mitral valve and double outlet right ventricle

Pages
223–225
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The infant died before surgical intervention.

📌 3 Key Takeaways

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Objective & Hypothesis:Cor triatriatum is a rare congenital cardiac anomaly and association of this pathology with Ebstein's malformation of atretic mitral valve and double outlet right ventricle has not been previously reported.
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Key Findings & Data:We present an 11-day-old infant with this unique anomaly diagnosed by echocardiographic examination.
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Conclusion & Impact:The infant died before surgical intervention.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Cor triatriatum is a rare congenital cardiac anomaly and association of this pathology with Ebstein's malformation of atretic mitral valve and double outlet right ventricle has not been previously reported. We present an 11-day-old infant with this unique anomaly diagnosed by echocardiographic examination. The infant died before surgical intervention.

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Cite This Article

ÖZTUNÇ, F., BEŞİKÇİ, R., AKALIN, F. (2022). Cor triatriatum associated with Ebstein malformation of atretic mitral valve and double outlet right ventricle. Marmara Medical Journal, Cilt: 13 - Sayı: 4, 223–225. https://ajindex.com/articles/578473

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