Abstract:
:Anomalous origin of the right coronary artery from the pulmonary artery, a rare congenital cardiac defect, is typically not diagnosed during infancy. On the other hand, Turner syndrome is usually diagnosed early, and it is classically associated with bicuspid aortic valve and aortic coarctation. Individuals with Turner syndrome are also at increased risk for coronary artery anomalies. We present a case of anomalous right coronary artery from the pulmonary artery in a week-old neonate who also had Turner syndrome, patent ductus arteriosus, transverse aortic arch hypoplasia, and impaired ventricular function. Prostaglandin therapy through the ductus increased the patient's myocardial perfusion. Four months after corrective surgery, she was doing well. We discuss the reperfusion phenomenon in our patient's case, as well as other considerations in this combination of congenital defects.
journal_name
Tex Heart Inst Jjournal_title
Texas Heart Institute journalauthors
Stefek BP,Imundo JR,Clark JBdoi
10.14503/THIJ-17-6521subject
Has Abstractpub_date
2019-06-01 00:00:00pages
225-228issue
3eissn
0730-2347issn
1526-6702journal_volume
46pub_type
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journal_title:Texas Heart Institute journal
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journal_title:Texas Heart Institute journal
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journal_title:Texas Heart Institute journal
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journal_title:Texas Heart Institute journal
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doi:
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pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Texas Heart Institute journal
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pub_type: 杂志文章,评审
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pub_type: 杂志文章
doi:
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