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the first report of the iranian combination of tetralogy of fallot and hypertrophic cardiomyopathy, a rare case report
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نویسنده
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ghasemi reza ,hosseinzadeh maleki mahmood ,yaghubi mohsen ,rahimpour feisal ,moradian maryam
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منبع
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journal of surgery and trauma - 2022 - دوره : 10 - شماره : 4 - صفحه:167 -171
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چکیده
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The tetralogy of fallot is the most common cyanotic congenital heart disease that is often associated with chromosomal aberration had a high prevalence rate of all congenital heart diseases. the association of the tetralogy of fallot (tof) with other congenital cardiac defects, especially with hypertrophic cardiomyopathy, is infrequent. while, unlike the tetralogy of fallot, hypertrophic cardiomyopathy is accompanied by specific gene loci.we report this scarce association in a 6-month male infant, cyanotic since birth and known with tof, in her first hospital admission for treatment of recurring cyanotic crises. after the preliminary evaluations and the unsuccessful stenting of the patent ductus arteriousus (pda) under an angiographic manner, he was prepared to undergo cardiac surgery to establish a modified blalock-taussig shunt procedure. the patient was discharged in good condition and suggested that his parents follow up on his cardiac function after it. on follow-up at the age of three, the child had no cyanotic crises in this period.
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کلیدواژه
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tetralogy of fallot ,hypertrophic cardiomyopathy ,congenital heart defects
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آدرس
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torbat heydariyeh university of medical sciences, 9 day hospital, department of cardiology, iran, mashhad university of medical sciences, imam reza hospital, department of cardiac surgery, iran, imam reza international university, razavi hospital, department of extra-corporeal circulation (ecc), iran, mashhad university of medical sciences, imam reza hospital, department of pediatric cardiology, iran, iran university of medical sciences, rajaie cardiovascular medical and research center, department of pediatric cardiology, iran
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پست الکترونیکی
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maryam_moradian2008@yahoo.com
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Authors
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