Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis | oneAMYLOIDOSISvoice

Trusted Resources: Education

Scientific literature and patient education texts

Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis

key information

source: Journal of the American College of Cardiology

year: 2015

authors: Gertz MA, Benson MD, Dyck PJ, Grogan M, Coelho T, Cruz M, Berk JL, Plante-Bordeneuve V, Schmidt HHJ, Merlini G

summary/abstract:

Transthyretin amyloidosis is a fatal disorder that is characterized primarily by progressive neuropathy and cardiomyopathy. It occurs in both a mutant form (with autosomal dominant inheritance) and a wild-type form (with predominant cardiac involvement). This article guides clinicians as to when the disease should be suspected, describes the appropriate diagnostic evaluation for those with known or suspected amyloidosis, and reviews the interventions currently available for affected patients.

organization: Mayo Clinic, USA; Indiana University School of Medicine, USA; Mayo Clinic, USA; Hospital de Santo Antonio, Portugal; Federal University of Rio de Janeiro of Brazil, Brazil; Boston University School of Medicine, USA; University Hospital Henri Mondor, France; Universitätsklinikum Münster, Germany; University of Pavia, Italy

DOI: 10.1016/j.jacc.2015.09.075

read more full text

To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences.
More information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close