Progression of QRS duration: a potential surrogate marker of survival in ATTRwt amyloidosis patients
In wild-type transthyretin amyloidosis (ATTRwt), the deposition of transthyretin in the myocardium leads to progressive heart failure. However, little is known about the short-term natural progression of this disease and potential predictors of outcome.
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| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
20 October 2025
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| In: |
Orphanet journal of rare diseases
Year: 2025, Jahrgang: 20, Heft: 1, Pages: 1-9 |
| ISSN: | 1750-1172 |
| DOI: | 10.1186/s13023-025-04078-4 |
| Online-Zugang: | Resolving-System, kostenfrei, Volltext: https://doi.org/10.1186/s13023-025-04078-4 Verlag, kostenfrei, Volltext: https://link.springer.com/article/10.1186/s13023-025-04078-4 
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| Verfasserangaben: | Selina Hein, Fabian aus dem Siepen, Sonja M. Zierleyn, Maximilian Knoll, Hugo A. Katus, Norbert Frey, Arnt V. Kristen |
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| 520 | |a In wild-type transthyretin amyloidosis (ATTRwt), the deposition of transthyretin in the myocardium leads to progressive heart failure. However, little is known about the short-term natural progression of this disease and potential predictors of outcome. | ||
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