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Journals / The European Research Journal / 2017 / Cilt: 3 - Sayı: 1

Class I pentalogy of Cantrell: a rare case report

Bayram Ali DORUM
Hilal ÖZKAN
Nilgün KÖKSAL
Yasemin Denkboy ONGEN
Pages
83–86
DOI
—
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AI Summary & Key Takeaways

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

We report here a case of class I Cantrell syndrome and our aim is to share difficulties experienced and review the related literature.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Pentalogy of Cantrell is characterized by the presence of five major congenital defects involving the abdominal wall, pericardium, diaphragm, lower sternum and various cardiac abnormalities.
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Key Findings & Data:This rare syndrome was described by Cantrell in 1958 and it has poor prognosis.
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Conclusion & Impact:We report here a case of class I Cantrell syndrome and our aim is to share difficulties experienced and review the related literature.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Cantrell syndrome · ectopia cordis · omphalocele

Abstract

Pentalogy of Cantrell is characterized by the presence of five major congenital defects involving the abdominal wall, pericardium, diaphragm, lower sternum and various cardiac abnormalities. This rare syndrome was described by Cantrell in 1958 and it has poor prognosis. We report here a case of class I Cantrell syndrome and our aim is to share difficulties experienced and review the related literature.

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Cite This Article

DORUM, B. A., ÖZKAN, H., KÖKSAL, N., ONGEN, Y. D. (2017). Class I pentalogy of Cantrell: a rare case report. The European Research Journal, Cilt: 3 - Sayı: 1, 83–86. https://ajindex.com/articles/361291

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References (9)

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