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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).

Fábio Fernandes | Georgina Del Cisne Jadán Luzuriaga | Guilherme Wesley Peixoto da Fonseca | Edileide Barros Correia | Alzira Alves Siqueira Carvalho | Ariane Vieira Scarlatelli Macedo | Otavio Rizzi Coelho-Filho | Phillip Scheinberg | Murillo Oliveira Antunes | Pedro Vellosa Schwartzmann | Sandrigo Mangini | Wilson Marques | Marcus Vinicius Simões
Orphanet journal of rare diseases | 2024

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 genetic profile of patients enrolled in the Transthyretin Cardiac Amyloidosis Registry of the State of São Paulo, Brazil.

Pubmed ID: 39033298

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Associated grants

  • Agency: Pfizer Foundation,
    Id: 68322757

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