Arrhythmias in patients with X-linked myotubular myopathy.

ABSTRACT:

Introduction

Myotubular myopathy is a congenital muscle disease caused by a mutation in the myotubularin (MTM1) gene. The X-linked myotubular myopathy (XLMTM) affects males with early-onset symptoms such as muscle weakness, hypotonia, and respiratory distress. To our knowledge, cardiac involvement has not been previously described in this condition, in contrast to other types of congenital myopathies such as nemaline myopathy or core myopathy.

Case reports

We report two clinical cases of XLMTM that started with severe sinus bradycardia or auriculoventricular block from the first days of life, with pathologic 24-hours Holter monitoring in both cases. A primary cardiac affection was excluded by electrophysiological studies and normal heart rate was recovered with proper respir

SUBMITTER: Pons-Espinal M 

PROVIDER: S-EPMC10662247 | biostudies-literature | 2023 Aug

REPOSITORIES: biostudies-literature