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Lafora Disease: Report of a Rare Entity
Lafora disease is a rare, genetic, glycogen metabolism disorder inherited as autosomal recessive characterized by the presence of inclusion bodies, known as Lafora bodies, within the cytoplasm of the cells in the heart, liver, muscle, and skin. Lafora disease presents as a neurodegenerative disorder...
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| Publicat a: | Cureus |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Cureus
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7046017/ https://ncbi.nlm.nih.gov/pubmed/32140352 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.6793 |
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