nkx2-5 mutations in patients with nonsyndromic congenital heart disease

Background: congenital heart diseases (chd) are the most common of all birth defects, affecting nearly 0.9% of all live births. nkx2-5 mutations were reported to cause chd but data in kurdish populations of iran are limited. objectives: in this experimental study, weperformed high resolution melt (hrm) mutation scanning of nkx2-5 exons of non-syndrome patients. patientsandmethods: thirty nine patients with atrial septal defectand57 patients with ventricular septal defect, 4 patients possessing both defects as case groups and 50 healthy controls. then we grouped samples according tohrmgraph and sequenced several samples from each group. results: hrmanalysis showed 2 deviated curves for exon 1 and one group for exon 2a and exon 2b. then, 2 samples of exon 1 that showed different hrm curves, 3 samples of another group from this exon and 5 samples of exon 2a, 2b and healthy controls were randomly sequenced. the results of sequencingconfirmedthehrmanalysis, andonepolymorphism(a65g)wasidentified in 2 atrial septal defects with deviated curves. conclusions: the environmental and effective factors on the heart development within embryonic evolution as well as the possibility of the existence of the mutation in coding genes of the other cardiac transcription factors such asgata4 and tbx5 can be the reasons for the lack of the pathogenic mutation in this study. it is suggested in further related studies to investigate normal and abnormal cardiac tissue samples of these studied patients and coding genes of the other cardiac transcription factors.