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. 2022 May 19;10(7):e1962. doi: 10.1002/mgg3.1962

FIGURE 1.

FIGURE 1

PRKAG2 variants in the two families. (a) Family pedigree revealing no carrier of PRKAG2 c.425C > T (p.T142I). The current proband (Case 1) exhibited severe DCM with a de novo heterozygous variant of PRKAG2 c.425C > T. (b) Echocardiography of the current proband, showing severe dilation of left ventricle. (c) ECG of the proband (c.425C > T), showing frequent ventricular pre‐mature beats. (d) Family pedigree revealing no carrier of PRKAG2 c.869A > T (p.K290I). The current proband (Case 2) exhibited severe HCM with de novo heterozygous variant of PRKAG2 c.869A > T. (e) Echocardiography in the current proband, showing a severe hypertrophy of left ventricle. (f) ECG of the proband (c.869A > T), showing ventricular preexcitation