A clinical case of hereditary transthyretin amyloidosis. Case report

For several years, there has been a significant increase in the number of patients diagnosed with cardiac amyloidosis. However, there are still difficulties associated with the diagnosis, identifying its type and further treatment of the disease. The diversity of the clinical symptoms, the absence o...

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Bibliographic Details
Main Authors: Anastasia A. Shoshina, Svetlana N. Nasonova, Igor V. Zhirov, Marina A. Saidova, Alexey A. Ansheles, Aleksei N. Meshkov, Sergey N. Tereshchenko
Format: Article
Language:Russian
Published: ZAO "Consilium Medicum" 2023-05-01
Series:Consilium Medicum
Subjects:
Online Access:https://consilium.orscience.ru/2075-1753/article/viewFile/420436/124868

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