Risk of Cardiac Arrhythmias in Patients with Late-Onset Pompe Disease—Results from a Long Follow-Up in a Group of 12 Patients and Review of Literature

<b>Background</b>. Pompe disease is a rare, severe, autosomal recessive genetic disorder caused by <i>GAA</i> gene mutations, which cause α-1,4-glucosidase enzyme deficiency. There are two forms of Pompe disease based on the age of onset, the infantile and the adult form (LOP...

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Bibliographic Details
Main Authors: Alberto Palladino, Luigia Passamano, Marianna Scutifero, Salvatore Morra, Esther Picillo, Andrea Antonio Papa, Gerardo Nigro, Luisa Politano
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:Cardiogenetics
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Online Access:https://www.mdpi.com/2035-8148/14/1/3