Arritmias en pacientes con miopatía miotubular ligada al cromosoma X

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...

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Detalles Bibliográficos
Autores principales: Pons-Espinal, Marina, Clotet-Caba, Jordi, Cesar-Díaz, Sergi, Yubero-Siles, Delia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: EVIDENZE 2023
Materias:
Nota Clínica
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662244/
http://dx.doi.org/10.33588/rn.7703.2022222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662244/
http://dx.doi.org/10.33588/rn.7703.2022222

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