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. 2013 Jun;68(6):777–784. doi: 10.6061/clinics/2013(06)09

Table 2.

Phenotypic characteristics and the Nkx2.5 mutation status of the affected pedigree members.

Subject Information Phenotype Electrocardiogram Echocardiogram Genotype
Identity Gender Age at time of study (years) Age at first diagnosis of AF (years) AF (classification) QRS interval (ms) QT/QTc LAD (mm) LVEF (%) Nkx2.5 mutations
Family 1 N19D
II-1 M 52 45 Long-lasting persistent 98 396/465 38 65 +/–
Family 2 F186S
I-1 M 65a 46 Long-lasting persistent 120 408/427 46 58 N/A
II-1 M 46 32 Persistent 110 388/450 42 65 +/–
II-5 M 40 35 Paroxysmal 104 438/482 40 62 +/–
II-8 F 38 38 Paroxysmal 88 418/424 37 68 +/–
III-2 M 22 22 Paroxysmal 86 382/424 32 64 +/–

Note: AF  =  atrial fibrillation; F  =  female; M  =  male; N/A  =  not available or not applicable; LAD  =  left atrial dimension; LVEF  =  left ventricular ejection fraction; QT  =  QT interval; QTc  =  corrected QT interval. + indicates present and – denotes absent. a Age at death.