Can an electrophysiologist play a role in diagnosing skeletal myopathy? A case of fukutin-related protein (cardio)myopathy
Dilated cardiomyopathy (DCM) is characterized by left ventricular enlargement and systolic dysfunction resulting from a broad spectrum of genetic and non-genetic etiologies.The primary question is whether DCM in a specific case represents an isolated phenotype or is a part of a broader syndrome.A 46-year-old man, working as a construction worker, was admitted to our heart failure (HF) outpatient clinic due to low left ventricular ejection fraction (LVEF) despite quadruple HF therapy.The patient had a history of bronchial asthma and a serious fall resulting in
Authors
- Michał Bohdan (ORCID: https://orcid.org/0000-0002-3496-2238)
- Maciej Kempa (ORCID: https://orcid.org/0000-0002-3472-2883)
- Szymon Budrejko (ORCID: https://orcid.org/0000-0002-5254-0813)
- Aleksandra Gintowt-Chakour
- Agnieszka Zienciuk‐Krajka (ORCID: https://orcid.org/0000-0002-1341-9893)
- Magdalena Chylińska (ORCID: https://orcid.org/0000-0002-9374-3430)
- Ludmiła Daniłowicz
- Kamil Suszczyński
Institutions
- ZRE Gdańsk (Poland) (PL)
- University Clinical Centre (PL)
- Gdańsk Medical University (PL)
Publication Details
- Journal
- Kardiologia Polska
- Published
- 2026-08-27
- DOI
- https://doi.org/10.33963/v.phj.114472
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00