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...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2024-02-01
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Series: | Cardiogenetics |
Subjects: | |
Online Access: | https://www.mdpi.com/2035-8148/14/1/3 |