Anomalous Left Coronary Artery from Pulmonary Artery presenting associated with Isolated Cleft Palate

سال انتشار: 1392
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 306

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شناسه ملی سند علمی:

JR_INTJMI-3-2_007

تاریخ نمایه سازی: 15 مهر 1398

چکیده مقاله:

Anomalous Left Coronary Artery from the pulmonary artery (ALCAPA) is a rare congenitalcardiac anomaly accounting for approximately 0.25%-0.5% of all congenital heart diseases. This anomalyis usually isolated, but has been associated with patent ductus arteriosus (PDA), ventricular septal defect(VSD), tetralogy of fallot (TOF) or coarctation of the aorta (COA). This anomaly hasn t been associatedwith extracardiac anomaly.Here we reported a 2-year of old male with cleft palate and the ALCAPA, whopresented with cardiomegaly and patent ductus arteriosus. As the early diagnosis of ALCAPA isimportant, we suggest this association consider in the cleft palate population with congenital heartdisease. AS the delay of ALCAPA diagnosis may be associated to elevated mortality and morbidity ofcleft palate repair, we suggest ALCAPA association was carefully searched in the cleft palate population.

کلیدواژه ها:

Anomalous left coronary artery ، pulmonary artery ، patent ducts arteriosus ، cleft palate

نویسندگان

Asadollah Tansan

Department of Pediatric, Faculty of Medicine, Hamadan University of Medical Sciences and Health Services, Hamadan, Iran

Ahmad Jamei Khosroshaei

Department of Pediatric, Faculty of Medicine, Tabriz University of Medical Sciences and Health Services, Tabriz, Iran

Farshad Rostampour

Student Research Committee (SRC), Faculty of Medicine, Hamadan University of Medical Sciences and HealthServices, Hamadan, Iran

Poya Tanasan

Medical Student, Faculty of Medicine, Tehran University of Medical Sciences and Health Services, Tehran, IranCorresponding author