Parallel Neurological and Cardiac Progression in Hereditary Transthyretin Amyloidosis: An Integrated Clinical and Imaging Study

<b>Background:</b> Hereditary transthyretin amyloidosis (ATTRv) is a rare, autosomal dominant multisystem disease caused by pathogenic variants in the transthyretin (TTR) gene. Although ATTRv is classically categorized into “cardiac” and “neurologic” phenotypes, recent evidence suggests a more compl...

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Autors principals:	Grazia Canciello, Stefano Tozza, Leopoldo Ordine, Brigida Napolitano, Giovanni Palumbo, Mariagiovanna Castiglia, Daniela Pacella, Raffaella Lombardi, Giovanni Esposito, Fiore Manganelli, Maria-Angela Losi
Format:	Artigo
Idioma:	Inglês
Publicat:	MDPI AG 2025-08-01
Col·lecció:	Diagnostics
Matèries:	hereditary transthyretin amyloidosis peripheral neuropathy global longitudinal strain neurological staging diastolic disfunction
Accés en línia:	https://www.mdpi.com/2075-4418/15/17/2143
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