Immunoglobulin Light-Chain Amyloidosis: Clinical Presentations and Diagnostic Approach

Systemic immunoglobulin light-chain (AL) amyloidosis is a rare disorder arising from a plasma cell clone that produces misfolded immunoglobulin light chains, which are deposited in various tissues and organs as amyloid fibrils. Signs and symptoms are typically vague and overlap with those arising fr...

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Detalles Bibliográficos
Autores principales: Hwa, Yi L., Fogaren, Teresa, Sams, Allison, Faller, Douglas V., Stull, Dawn M., Thuenemann, Sara, Mendelson, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Harborside Press LLC 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779572/
https://www.ncbi.nlm.nih.gov/pubmed/33457060
http://dx.doi.org/10.6004/jadpro.2019.10.5.5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779572/
https://www.ncbi.nlm.nih.gov/pubmed/33457060
http://dx.doi.org/10.6004/jadpro.2019.10.5.5

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