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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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| Publicado no: | J Cardiovasc Magn Reson |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5146906/ https://ncbi.nlm.nih.gov/pubmed/27931223 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12968-016-0311-9 |
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