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Dilate kardiyomiyopatili bir olguda tanımlanan Bland-White-Garland sendromu

Bland-White-Garland syndrome in an infant with dilated cardiomyopathy

Journal Name:

  • Gülhane Tıp Dergisi

Publication Year:

  • 2007

Key Words:

Keywords (Original Language):

Author Name
Abstract (2. Language): 
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.
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Abstract (Original Language): 
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.
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  • 3
187-190
  • Turkish

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