First Report of Lysozyme Amyloidosis with p.F21L/T88N Amino Acid Substitutions in a Russian Family

First Report of Lysozyme Amyloidosis with p.F21L/T88N Amino Acid Substitutions in a Russian Family

Lysozyme amyloidosis is caused by an amino acid substitution in the sequence of this protein. In our study, we described a clinical case of lysozyme amyloidosis in a Russian family. In our work, we described in detail the histological changes in tissues that appeared as a result of massive depositio...

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Bibliographic Details
Main Authors: Mariya Yu. Suvorina, Elena A. Stepanova, Vilen V. Rameev, Lidiya V. Kozlovskaya, Anatoly S. Glukhov, Anastasiya A. Kuznitsyna, Alexey K. Surin, Oxana V. Galzitskaya
Format: Article
Language:English
Published: MDPI AG 2023-09-01
Series:International Journal of Molecular Sciences
Subjects:
genetic testing
hereditary systemic amyloidosis
histology
lysozyme amyloidosis
mass spectrometry
Online Access:https://www.mdpi.com/1422-0067/24/19/14453

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