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Published online: 2024-12-03

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Atrial standstill phenomenon in non-dilated cardiomyopathy phenotype of genetically confirmed laminopathy

Klaudia Męcka1, Paweł Bańka1, Bartosz Gruchlik1, Piotr Kukla2, Katarzyna Mizia-Stec1

Abstract

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References

  1. Biernacka EK, Osadnik T, Bilińska ZT, et al. Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities. Pol Heart J. 2024; 82(5): 569–593.
  2. Zhang Y, Zhang Y, Ren M, et al. Atrial standstill associated with lamin A/C mutation: A case report. SAGE Open Med Case Rep. 2023; 11: 2050313X231179810.
  3. Ning S, Han M, Qiu R, et al. Novel pathogenic variant in LMNA gene identified in a six-generation family causing atrial cardiomyopathy and associated right atrial conduction arrhythmias. Front Cardiovasc Med. 2023; 10: 1109008.
  4. Marchel M, Madej-Pilarczyk A, Steckiewicz R, et al. Predictors of mortality and cardiovascular outcomes in Emery-Dreifuss muscular dystrophy in a long-term follow-up. Kardiol Pol. 2021; 79(12): 1335–1342.