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Fig. 3 | BMC Cardiovascular Disorders

Fig. 3

From: Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death

Fig. 3

Clinical courses. The patient in Case 1 (female, II-4, proband) presented with AF with bradycardia in her fifties, and polymorphic VT in her seventies. The elder sister (II-2) of the patient in Case 1, who did not undergo genetic testing, presented with SSS with PMI in her sixties, and died suddenly due to VF. The patient in Case 2 (male, III-1) presented with CAVB in his forties, and DCM and VT in his fifties. The patient in Case 3 (male, III-4) presented with AF, CAVB, DCM, and VT in his fifties. AF, atrial fibrillation; CAVB, complete atrioventricular block; CRTD, cardiac resynchronization therapy defibrillator; DCM, dilated cardiomyopathy; LVEF, left ventricular ejection fraction; PMI, pacemaker implantation; SCD, sudden cardiac death; SSS, sick sinus syndrome; VF, ventricular fibrillation; VT, ventricular tachyarrhythmia

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