Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis

Abstract Background Hereditary transthyretin (ATTRv) amyloidosis is rare, autosomal dominant disease with a fatal outcome if left untreated. Early stages detection is crucial for intervention. We aimed identifying early indexes of cardiac involvement and their eventual correlation with neurological...

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Main Authors: Grazia Canciello, Stefano Tozza, Gaetano Todde, Maria Nolano, Felice Borrelli, Giovanni Palumbo, Raffaella Lombardi, Emanuele Cassano, Wanda Acampa, Giovanni Esposito, Fiore Manganelli, Maria Angela Losi
Format: Article
Language:English
Published: BMC 2024-12-01
Series:Orphanet Journal of Rare Diseases
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Online Access:https://doi.org/10.1186/s13023-024-03473-7
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