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. 2022 Jan 1;118(1):106–109. [Article in Portuguese] doi: 10.36660/abc.20210062

Table 1. Clinical features of the study patients (n=16), members of a single family with an Arg302Gln mutation in PRKAG2 gene.

Patient Sex Age (years) Age at onset of symptoms (years) Sudden death CID LVH
II:8 F 38† - + - NA
II:9 M 40† - + - NA
III:23 M 28† 28 + - NA
II:5 M 56 30 - PM +
II:6 M 60† 42 - PM +
II:7 F 58 40 - PM +
II:10 M 53 44 - PM +
III:8 F 43 23 - ICD +
III:15 M 31 26 - PM -
III:16 F 33 33 - - -
III:18 M 43 39 - - -
III:21 M 39 33 - - +
III:22 F 35 - - - -
III:24 M 35 - - - -
III:27 M 35 28 - - +
III:28 F 20 - - - -
+

present; -: absent; NA: not available;

deceased; M: male; F: female; CID: cardiac implantable device; PM: pacemaker; ICD: implantable cardioverter-defibrillator; LVH: left ventricular hypertrophy.