A patient with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA syndrome) and 13 live births
العنوان: | A patient with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA syndrome) and 13 live births |
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المؤلفون: | Mustafa Kemal Avsar, Mustafa Yolcu, Mehmet Salih Bilal, Ozgur Yildirim |
بيانات النشر: | NLM (Medline), 2019. |
سنة النشر: | 2019 |
مصطلحات موضوعية: | ALCAPA Syndrome, medicine.medical_specialty, Pregnancy, business.industry, Mortality rate, General Medicine, medicine.disease, Asymptomatic, Left coronary artery, Internal medicine, medicine.artery, Heart failure, Right coronary artery, Surgical, Pulmonary artery, medicine, Cardiology, medicine.symptom, Cardiology and Cardiovascular Medicine, business, Live birth, Live Birth |
الوصف: | Yolcu, Mustafa (Arel Author) --- PubMed ID: 30729975 Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) or Bland-White-Garland syndrome is a rarely seen congenital anomaly. Adult and infantile types are defined according to the degree of collateral development between the left coronary artery (LCA) and right coronary artery (RCA). If left untreated, ALCAPA has a 90% mortality rate in the first year of life, primarily due to myocardial ischaemia and heart failure. The degree of collateral development and the related LCA perfusion in ALCAPA syndrome determine the occurrence of symptoms. Herein, we present a case of a female patient who had previously, without any symptoms, given live birth to 13 babies. She had been experiencing exertional angina, which started long after the delivery of her 13th child. Since our patient had well-developed collaterals to the LCA, she was asymptomatic and able to give birth to the children via the vaginal route without any problems. Having well-formed collateral vessels between the RCA and LCA may prevent patients from developing symptoms, and even stressful conditions such as pregnancy may be tolerable. |
وصف الملف: | application/pdf |
اللغة: | English |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47a3d145fbbec1aa71d1b49ffdb1b2c https://hdl.handle.net/20.500.12294/1891 |
حقوق: | OPEN |
رقم الأكسشن: | edsair.doi.dedup.....c47a3d145fbbec1aa71d1b49ffdb1b2c |
قاعدة البيانات: | OpenAIRE |
الوصف غير متاح. |