Phenotypic Presentation and Longitudinal Characterization of Hereditary ATTRv Amyloidosis in Previously Undiagnosed Family Members
Background: Clinical characteristics, cardiac disease progression, and outcomes of “previously undiagnosed” family members of patients with hereditary transthyretin amyloid cardiomyopathy (ATTRv-CM) with pathogenic or likely pathogenic transthyretin (TTR) variants (genotype positive or G+) are unkno...
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Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2025-08-01
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Series: | JACC: Advances |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2772963X25004600 |
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