Autor: |
Hajar El Ouartassi, MD, Raid Faraj, MD, Zakariae Laraichi, MD, Rhita Ezzahraoui, MD, Zaineb Bourouhou, MD, Nawal Doghmi, PhD, Mohamed Cherti, PhD |
Jazyk: |
angličtina |
Rok vydání: |
2023 |
Předmět: |
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Zdroj: |
Radiology Case Reports, Vol 18, Iss 9, Pp 3248-3251 (2023) |
Druh dokumentu: |
article |
ISSN: |
1930-0433 |
DOI: |
10.1016/j.radcr.2023.06.034 |
Popis: |
Arrhythmogenic cardiomyopathy is a genetic heart muscle disease that typically affects the right ventricle. However, 2 other phenotypes affecting the left ventricle were recently discovered. Here, we report the case of an 18-year-old patient with biventricular arrhythmogenic cardiomyopathy, highlighting the challenges encountered in establishing this diagnosis. Diagnostic criteria for the left-sided phenotypic variants of arrhythmogenic cardiomyopathy were only introduced in 2020 by an international expert consensus document, known as the “Padua criteria,” they are divided in 6 categories with an emphasis on morpho-functional ventricular abnormalities and structural myocardial tissue alterations to diagnose biventricular arrhythmogenic cardiomyopathy. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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