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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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Bibliographic Details
Published in:Iberoamerican Journal of Medicine
Main Authors: Salem Bouomrani, Fahd Saadaoui, Nour Elhouda Ayadi
Format: Artigo
Language:Inglês
Published: Hospital San Pedro 2021
Subjects:
Online Access: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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