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Retinitis pigmentosa associated with systemic light chain amyloidosis (AL amyloidosis)
Retinitis pigmentosa (RP) or hereditary retinal dystrophy is a rare disease that can be isolated (non-syndromic RP) or associated with other systemic signs (syndromic RP). Kidney damage is exceptionally reported in patients with RP, particularly in syndromic forms. Association with renal amyloidosis...
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| Vydáno v: | Iberoamerican Journal of Medicine |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hospital San Pedro
2021
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| Témata: | |
| On-line přístup: | https://www.redalyc.org/articulo.oa?id=692072542011 https://www.redalyc.org/journal/6920/692072542011/ https://www.redalyc.org/journal/6920/692072542011/html/ https://www.redalyc.org/journal/6920/692072542011/692072542011.epub https://www.redalyc.org/journal/6920/692072542011/movil https://doi.org/10.5281/zenodo.4655879 |
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