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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| Auteurs principaux: | , , |
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| Format: | article |
| Langue: | EN |
| Publié: |
Emergency Department of Hospital San Pedro (Logroño, Spain)
2021
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| Accès en ligne: | https://doaj.org/article/8e83e686ba134940979a1a0f5beff8d0 |
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