Pattern and prognostic value of cardiac involvement in patients with late-onset pompe disease: a comprehensive cardiovascular magnetic resonance approach

BACKGROUND: Pompe disease is an autosomal recessive disorder caused by deficiency of the lysosomal α–1,4-glucosidase leading to accumulation of glycogen in target tissues with progressive organ failure. While the early infantile-onset form is characterized by early severe hypertrophic cardiomyopathy...

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Detalles Bibliográficos
Autores principales: Boentert, Matthias, Florian, Anca, Dräger, Bianca, Young, Peter, Yilmaz, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146906/
https://www.ncbi.nlm.nih.gov/pubmed/27931223
http://dx.doi.org/10.1186/s12968-016-0311-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146906/
https://www.ncbi.nlm.nih.gov/pubmed/27931223
http://dx.doi.org/10.1186/s12968-016-0311-9

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