دوره 10، شماره 4 - ( 10-1401 )
جلد 10 شماره 4 صفحات 171-167 |
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Rahimpour F, Ghasemi R, Moradian M, Hosseinzadeh Maleki M, Yaghubi M. The first report of the iranian combination of tetralogy of fallot and hypertrophic cardiomyopathy, A rare case report. J Surg Trauma 2022; 10 (4) :167-171
URL: http://jsurgery.bums.ac.ir/article-1-326-fa.html
URL: http://jsurgery.bums.ac.ir/article-1-326-fa.html
The first report of the iranian combination of tetralogy of fallot and hypertrophic cardiomyopathy, A rare case report. نشریه جراحی و تروما 1401; 10 (4) :171-167
چکیده: (557 مشاهده)
- 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.
نوع مطالعه: گزارش مورد |
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جراحی قلب
دریافت: 1400/11/16 | پذیرش: 1401/3/25 | انتشار الکترونیک پیش از انتشار نهایی: 1401/6/11 | انتشار: 1401/10/8 | انتشار الکترونیک: 1401/10/8
دریافت: 1400/11/16 | پذیرش: 1401/3/25 | انتشار الکترونیک پیش از انتشار نهایی: 1401/6/11 | انتشار: 1401/10/8 | انتشار الکترونیک: 1401/10/8
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