Cardiogenetics MDPI

Aino-Maija Vuorinen et al. indicate that the genetic testing of MELAS should be considered in new cases of HCM or sudden heart failure phenotypes of unknown etiology.

Check it here:

Cardiac Involvement in Patients with MELAS-Related mtDNA 3243A>G Variant Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare disease with variable clinical manifestations. MELAS is most often caused by the human mitochondrial DNA (mtDNA) m.3243A>G variant. We describe cardiac magnetic resonance (CMR) imaging findin...

Antonio Concistrè et al. about their new review in Cardiogenetics: we propose a 3-category genetic framework for endocrine-related cardiomyopathies — from somatic mutations to pleiotropy & precision medicine.

https://brnw.ch/21x1pGr