Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease

Congenital heart disease (chd) is the most common birth defect occurring in humans and some transcriptional factors have been identified as causative. however, additional mutation analysis of these genes is necessary to develop effective diagnostic and medical treatment methods. we conducted sequence analysis of the coding regions of nkx2.5, gata4, tbx1, tbx5, tbx20, cfc1 and zic3 in 111 japanese patients with non-syndromic chd and 9 of their relatives. all patient samples were also analyzed by multiplex ligation-dependent probe amplification using probes involved in chromosome deletion related to chd. five novel variations of tbx5, gata4 and tbx20 were detected in 6 of the patients, whereas none were found in 200 controls. the tbx5 variation p.pro108thr, located in the t-box domain, was identified in a patient with tricuspid atresia, an exon–intron boundary variation of gata4 (ivs4+5g>a) was detected in a tetralogy of fallot patient and an 8p23 microdeletion was detected in one patient with atrioventricular septal defect and psychomotor delay. a total of seven non-synonymous polymorphisms were found in the patients and controls. accumulation of novel variations of genes involving the cardiac development may be required for better understanding of chd.