Cardiac manifestations of PRKAG2 mutation.
Pooya BanankhahGregory A FishbeinAnthony DotaReza ArdehaliPublished in: BMC medical genetics (2018)
The pathologic and genetics findings of our patient are consistent with PRKAG2 syndrome. Patients presenting with conduction abnormalities and suspected HCM should be considered for genetic testing to identify possible underlying genetic etiologies.