<i>PRKAG2</i> Syndrome: Clinical Features, Imaging Findings and Cardiac Events

<i>PRKAG2</i> Syndrome: Clinical Features, Imaging Findings and Cardiac Events

<b>Background/Objectives:</b> <i>PRKAG2</i> syndrome (PS) is a rare genocopy of hypertrophic cardiomyopathy (HCM). Our goal was to expand knowledge about PS by analyzing patient clinical, imaging, and follow-up data. <b>Methods</b>: The study included carriers of...

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Main Authors: Maria Sudomir, Przemysław Chmielewski, Grażyna Truszkowska, Mariusz Kłopotowski, Mateusz Śpiewak, Marta Legatowicz-Koprowska, Monika Gawor-Prokopczyk, Justyna Szczygieł, Joanna Zakrzewska-Koperska, Mariusz Kruk, Jolanta Krzysztoń-Russjan, Jacek Grzybowski, Rafał Płoski, Zofia T. Bilińska
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Biomedicines
Subjects:
cardiomyopathy
hypertrophic
genetics
next generation sequencing
cardiac magnetic resonance
endomyocardial biopsy
Online Access:https://www.mdpi.com/2227-9059/13/3/751
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