Mixed-Etiology Restrictive Cardiomyopathy (Desminopathy and Hemochromatosis) with Complex Liver Lesions
A 28 year-old male with restrictive cardiomyopathy (RCM) and endocardium thickening, conduction disorders, heart failure, and depressive disorder treated with paroxetine was admitted to the clinic. Blood tests revealed an increase in serum iron level, transferrin saturation percentage, and slightly...
Main Authors: | Yulia Lutokhina, Olga Blagova, Alexander Panferov, Vsevolod Sedov, Evgeniya Kogan, Tatiana Nekrasova, Alexander Nedostup, Elena Zaklyazminskaya |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-03-01
|
Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/13/4/577 |
Similar Items
-
Hemochromatosis gene mutations in the general population of Slovakia
by: Gabriková Dana, et al.
Published: (2011-04-01) -
Pathogenesis, Diagnosis, and Clinical Implications of Hereditary Hemochromatosis—The Cardiological Point of View
by: Ludmiła Daniłowicz-Szymanowicz, et al.
Published: (2021-07-01) -
HFE hemochromatosis: an overview about therapeutic recommendations
by: Rodolfo D. Cancado, et al.
Published: (2022-01-01) -
<i>HIF1A:</i> A Putative Modifier of Hemochromatosis
by: Sara Pelucchi, et al.
Published: (2021-01-01) -
Therapeutic Erythrocytapheresis in the Initial Treatment of Hereditary Hemochromatosis
by: Vít Řeháček, et al.
Published: (2012-01-01)