Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP)

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Transthyretin amyloidosis (ATTR) is a multisystem disease caused by the deposition of fibrillar protein in organs and tissues. ATTR genotypes and phenotypes are highly heterogeneous. We present data on physical signs and symptoms, cardiac and neurological assessments and genetics in patients enrolled in the Transthyretin Cardiac Amyloidosis Registry in the state...

Topics

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• Aged
• Amyloid Neuropathies, Familial
• Brazil
• Genotype
• Mutation
• Phenotype
• Prealbumin
• Registries

Identifiers and source

Literature Corpus work

bfff3a34-a826-56ea-b3b8-8826e2009964

DOI

10.21203/rs.3.rs-4021958/v1