Yenidoğan döneminde dilate kardiyomiyopatinin nadir bir nedeni: ALCAPA sendromu

Babaoğlu, Kadir; Binnetoğlu, Köksal; Altun, Gürkan; Çetin, Gürel; Saltık, Levent

doi:10.4274/tpa.46.84

tpa

2011

DOI: 10.4274/tpa.46.84

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Yenidoğan döneminde dilate kardiyomiyopatinin nadir bir nedeni: ALCAPA sendromu

Kadir Babaoğlu¹,

Köksal Binnetoğlu²,

Gürkan Altun³

et al.

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2013

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“…A few such pediatric cases have been reported from Turkey. [2][3][4] In this case report, an 11-year-old girl presented with findings of ALCAPA in echocardiography (ECHO), multi-slice computed tomography (MSCT) and coronary angiography. The report aims at emphasizing the importance of keeping this syndrome in mind in patients with dilated cardiomyopathy (DCM).…”

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confidence: 99%

Anomalous origin of the left coronary artery from the pulmonary artery presenting as dilated cardiomyopathy

2013

Arch Turk Soc Cardiol

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Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly and one of the causes of myocardial ischemia. It often presents with atypical signs and symptoms, especially in childhood. In this case report, an 11-year-old girl presented with dilated cardiomyopathy in our clinic and was followed for five years. Echocardiography showed multiple left-to-right shunts on the interventricular septum, the confirmation of which was done by multi-slice computed tomography and coronary angiography. Therefore, we suggest that ALCAPA should be suspected in young patients diagnosed with dilated cardiomyopathy.

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mentioning

confidence: 99%

Anomalous origin of the left coronary artery from the pulmonary artery presenting as dilated cardiomyopathy

2013

Arch Turk Soc Cardiol

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Yenidoğan döneminde dilate kardiyomiyopatinin nadir bir nedeni: ALCAPA sendromu

Cited by 1 publication

References 13 publications

Anomalous origin of the left coronary artery from the pulmonary artery presenting as dilated cardiomyopathy

Anomalous origin of the left coronary artery from the pulmonary artery presenting as dilated cardiomyopathy

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