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Chagasic cardiomyopathy and Pompe disease: case report
Background: Pompe disease is a lysosomal storage disease with an autosomal recessive inheritance characterized by an insufficient activity of the acid alpha-glucosidase enzyme. The incidence varies from 1:40000 to 1:200000 live births and cardiac involvement in adults is rare. Chagas disease is an i...
Tallennettuna:
| Julkaisussa: | Am J Cardiovasc Dis |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
e-Century Publishing Corporation
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5944812/ https://ncbi.nlm.nih.gov/pubmed/29755837 |
| Tagit: |
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