Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature

Hereditary transthyretin amyloidosis is caused by pathogenic variants (ATTR(v)) in the TTR gene. Alongside cardiac dysfunction, the disease typically manifests with a severely progressive sensorimotor and autonomic polyneuropathy. Three different drugs, tafamidis, patisiran, and inotersen, are appro...

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Detalles Bibliográficos
Autores principales: Dohrn, Maike F., Auer-Grumbach, Michaela, Baron, Ralf, Birklein, Frank, Escolano-Lozano, Fabiola, Geber, Christian, Grether, Nicolai, Hagenacker, Tim, Hund, Ernst, Sachau, Juliane, Schilling, Matthias, Schmidt, Jens, Schulte-Mattler, Wilhelm, Sommer, Claudia, Weiler, Markus, Wunderlich, Gilbert, Hahn, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463516/
https://www.ncbi.nlm.nih.gov/pubmed/32500375
http://dx.doi.org/10.1007/s00415-020-09962-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463516/
https://www.ncbi.nlm.nih.gov/pubmed/32500375
http://dx.doi.org/10.1007/s00415-020-09962-6

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