We herein present our 11-month-old case diagnosed to have and operated for ALCAPA since ALCAPA is an important and treatable cause of dilated cardiomyopathy in infants.
📌 3 Key Takeaways
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Objective & Hypothesis:Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) accounts for 0.023% of all congenital heart defects and is seen in every 30.000 to 300.000 live births.
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Key Findings & Data:Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) accounts for 0.023% of all congenital heart defects and is seen in every 30.000 to 300.000 live births.
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Conclusion & Impact:We herein present our 11-month-old case diagnosed to have and operated for ALCAPA since ALCAPA is an important and treatable cause of dilated cardiomyopathy in infants.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Kadın · Süt çocuğu · Sendrom
Abstract
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) accounts for 0.023% of all congenital heart defects and is seen in every 30.000 to 300.000 live births. We herein present our 11-month-old case diagnosed to have and operated for ALCAPA since ALCAPA is an important and treatable cause of dilated cardiomyopathy in infants.
Özet
ALCAPA (“Anomalous origin of the left coronary artery from the pulmonary artery”) doğumsal kalp hastalıklarının %0.023'ünü oluşturur ve canlı doğumlarda 1/30.000-300.000 sıklığında görülür. Süt çocuklarında dilate kardiyomiyopatinin önemli ve tedavi edilebilir bir nedeni olmasından dolayı 11 aylık iken tanı konularak opere edilen olgumuzu sunmayı uygun bulduk.
OKUTAN, V., YOZGAT, Y., LENK, M. K., KUŞAKLIOĞLU, H., ÖZAL, E., VARAN, B., TOKEL, K., AŞLAMACI, M. S. (2007). Bland-White-Garland syndrome in an infant with dilated cardiomyopathy. Gülhane Tıp Dergisi, Cilt: 49 - Sayı: 3, 187–190. https://ajindex.com/articles/225580
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