Development of late amyloid cardiomyopathy following liver transplantation for hereditary Val30Met transthyretin amyloidosis

Amyloid. 2021 Sep;28(3):215-216. doi: 10.1080/13506129.2021.1904391. Epub 2021 Apr 5.

Authors

Keerthi T Gondi¹, Salik Nazir², Robert Grande², Scott L Hummel³

Affiliations

¹ University of Michigan Division of Internal Medicine, Ann Arbor, MI.
² University of Toledo Medical Center Division of Cardiology, Toledo, OH.
³ University of Michigan Division of Cardiovascular Medicine, Section of Cardiology, Ann Arbor Veterans Affairs Health System, Ann Arbor, MI.

PMID: 33818235
DOI: 10.1080/13506129.2021.1904391

No abstract available

Publication types

Letter
Comment

MeSH terms

Amyloid Neuropathies, Familial* / genetics
Amyloid Neuropathies, Familial* / surgery
Cardiomyopathies* / genetics
Cardiomyopathies* / surgery
Humans
Liver Transplantation*
Prealbumin / genetics

Substances

Prealbumin

Supplementary concepts

Amyloidosis, Hereditary, Transthyretin-Related