Journals / Türk Kardiyoloji Derneği Arşivi / 2019 / Cilt: 47 - Sayı: 4

Mosaic trisomy 14 and aorta-pulmonary window association: A case report

Mozaik trizomi 14 ve aorta-pulmoner pencere birlikteliği: Bir olgu sunumu

Pages
319–323
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

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

Trisomy 14 mosaicism is a rare chromosomalabnormality with distinct and recognizable clinical features.Congenital heart anomalies can accompany in this syndrome.To the best of our knowledge, this is the first caseof mosaic trisomy 14 with an aortopulmonary window to bedescribed in the literature.

📌 3 Key Takeaways

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Objective & Hypothesis:Trisomy 14 mosaicism is a rare chromosomalabnormality with distinct and recognizable clinical features.Congenital heart anomalies can accompany in this syndrome.To the best of our knowledge, this is the first caseof mosaic trisomy 14 with an aortopulmonary window to bedescribed in the literature.
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Key Findings & Data:Trisomy 14 mosaicism is a rare chromosomalabnormality with distinct and recognizable clinical features.Congenital heart anomalies can accompany in this syndrome.To the best of our knowledge, this is the first caseof mosaic trisomy 14 with an aortopulmonary window to bedescribed in the literature.
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Conclusion & Impact:Trisomy 14 mosaicism is a rare chromosomalabnormality with distinct and recognizable clinical features.Congenital heart anomalies can accompany in this syndrome.To the best of our knowledge, this is the first caseof mosaic trisomy 14 with an aortopulmonary window to bedescribed in the literature.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Trisomy 14 mosaicism is a rare chromosomalabnormality with distinct and recognizable clinical features.Congenital heart anomalies can accompany in this syndrome.To the best of our knowledge, this is the first caseof mosaic trisomy 14 with an aortopulmonary window to bedescribed in the literature.

Özet

Mozaik trizomi 14, belirgin ve tanınabilir klinik özelliklere sahip nadir bir kromozom anomalisidir. Bu sendroma doğuştan kalp anomalileri eşlik edebilmektedir. Bu olguda literatürde daha önce yer almayan aorta-pulmoner ile pencere mozaik trizomi 14 birlikteliğini sunuyoruz.

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Cite This Article

ALTUNHAN, H., YILMAZ, F. H., TARAKÇI, N., BAYSAL, T., OFLAZ, M. B. (2022). Mosaic trisomy 14 and aorta-pulmonary window association: A case report. Türk Kardiyoloji Derneği Arşivi, Cilt: 47 - Sayı: 4, 319–323. https://ajindex.com/articles/631852

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References (11)

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