The journey to diagnosis of wild-type transthyretin-mediated (ATTRwt) amyloidosis: a path with multisystem involvement

Abstract Background Wild-type and hereditary transthyretin-mediated amyloidosis (ATTRwt and ATTRv amyloidosis, respectively) are progressive, fatal diseases with a broad range of clinical presentations and multisystem effects. Despite having a higher prevalence, ATTRwt amyloidosis is less well chara...

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Hlavní autoři:	Chafic Karam, Colleen Moffit, Catherine Summers, Madeline P. Merkel, Fran M. Kochman, Laure Weijers, Mathilde Puls, Marieke Schurer, Emily Jones, Nicola Mason, Muriel Finkel, Paula Schmitt, Mazen Hanna
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2024-11-01
Edice:	Orphanet Journal of Rare Diseases
Témata:	Hereditary transthyretin-mediated amyloidosis Wild-type transthyretin-mediated amyloidosis hATTR wtATTR ATTRwt ATTRv
On-line přístup:	https://doi.org/10.1186/s13023-024-03407-3
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