Phenotypic Presentation and Longitudinal Characterization of Hereditary ATTRv Amyloidosis in Previously Undiagnosed Family Members
Previously undiagnosed ATTRv G+ family members have a greater prevalence and incidence of symptomatic neurological rather than cardiac disease, and the progression of cardiac disease was limited, which has implications for treating these patients preemptively.
Authors
- Angela A. Dispenzieri (ORCID: https://orcid.org/0000-0001-8780-9512)
- Naveen L. Pereira (ORCID: https://orcid.org/0000-0003-3813-3469)
- Luca Fazzini (ORCID: https://orcid.org/0000-0003-2407-7435)
- Marta Figueiral (ORCID: https://orcid.org/0000-0003-3308-774X)
- Christian Cadeddu Dessalvi (ORCID: https://orcid.org/0000-0002-2823-1797)
- Eric W. Klee (ORCID: https://orcid.org/0000-0003-2946-5795)
- Matteo Castrichini (ORCID: https://orcid.org/0000-0002-2405-3364)
- Martha Grogan (ORCID: https://orcid.org/0000-0002-2541-4440)
- Li Yan (ORCID: https://orcid.org/0000-0002-4792-9998)
- Jose De Melo
- Jenny J Cao
Institutions
- Mayo Clinic (US)
- University of Cagliari (IT)
- Mayo Clinic in Arizona (US)
- Mayo Clinic in Florida (US)
Publication Details
- Journal
- JACC Advances
- Published
- 2025-07-24
- DOI
- https://doi.org/10.1016/j.jacadv.2025.102036
- Citations
- 4
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 3.22
Funders
- Società Italiana di Cardiologia