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Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta
The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical Publishers
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502634/ https://www.ncbi.nlm.nih.gov/pubmed/26199806 http://dx.doi.org/10.1055/s-0035-1547331 |
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author | Zeng, Shi Zhou, Qichang Zhou, Jiawei Peng, Qinghai |
author_facet | Zeng, Shi Zhou, Qichang Zhou, Jiawei Peng, Qinghai |
author_sort | Zeng, Shi |
collection | PubMed |
description | The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have reported fetal anomalous origin of PA from aorta with other malformation. We report a case of isolated distal anomalous origin of the right PA from the aorta that was diagnosed by fetal echocardiography at 25 weeks' of gestation. Tracing the course of PA branches is important to make diagnosis. |
format | Online Article Text |
id | pubmed-4502634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Thieme Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-45026342015-07-21 Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta Zeng, Shi Zhou, Qichang Zhou, Jiawei Peng, Qinghai AJP Rep Article The anomalous origin of a branch pulmonary artery from the aorta (AOPA) is characterized by the anomalous origin of one of the branch pulmonary arteries (PA) from the ascending aorta and a normal origin of the other PA from main PA. AOPA is an extremely rare cardiac malformation. Few studies have reported fetal anomalous origin of PA from aorta with other malformation. We report a case of isolated distal anomalous origin of the right PA from the aorta that was diagnosed by fetal echocardiography at 25 weeks' of gestation. Tracing the course of PA branches is important to make diagnosis. Thieme Medical Publishers 2015-03-04 2015-04 /pmc/articles/PMC4502634/ /pubmed/26199806 http://dx.doi.org/10.1055/s-0035-1547331 Text en © Thieme Medical Publishers |
spellingShingle | Article Zeng, Shi Zhou, Qichang Zhou, Jiawei Peng, Qinghai Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta |
title | Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta |
title_full | Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta |
title_fullStr | Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta |
title_full_unstemmed | Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta |
title_short | Fetal Isolated Anomalous Origin of Right Pulmonary Artery from Aorta |
title_sort | fetal isolated anomalous origin of right pulmonary artery from aorta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502634/ https://www.ncbi.nlm.nih.gov/pubmed/26199806 http://dx.doi.org/10.1055/s-0035-1547331 |
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