Physiology, Diagnosis and Treatment of Cardiac Light Chain Amyloidosis

Physiology, Diagnosis and Treatment of Cardiac Light Chain Amyloidosis

AL (light-chain) amyloidosis is a systemic disease in which amyloid fibers are formed from kappa or lambda immunoglobulin light chains, or fragments thereof, produced by a neoplastic clone of plasmocytes. The produced protein is deposited in tissues and organs in the form of extracellular deposits,...

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Bibliographic Details
Main Authors: Agnieszka Stelmach-Gołdyś, Monika Zaborek-Łyczba, Jakub Łyczba, Bartosz Garus, Marcin Pasiarski, Paulina Mertowska, Paulina Małkowska, Rafał Hrynkiewicz, Paulina Niedźwiedzka-Rystwej, Ewelina Grywalska
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Journal of Clinical Medicine
Subjects:
amyloidosis
cardiac amyloidosis
light-chain amyloidosis
molecular mechanisms
protein aggregation
misfolding
Online Access:https://www.mdpi.com/2077-0383/11/4/911

Internet

https://www.mdpi.com/2077-0383/11/4/911

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