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Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology.

Volha SkrahinaUlrike GrittnerChristian BeetzThomas SkripuletzMartin JuenemannHeidrun H KrämerKatrin HahnAndreas RiethVolker SchaechingerMonica PattenChristian TanislavStephan AchenbachBirgit AssmusFabian KnebelStefan GingeleAliaksandr SkrahinJörg HartkampToni M FörsterSabine RoesnerCatarina PereiraArndt Rolfs
Published in: Annals of medicine (2021)
variant.Routine genetic testing is recommended in patients with unexplained CM and/or PNP to accelerate the initial diagnosis and timely treatment initiation.
Keyphrases
  • heart failure
  • clinical practice
  • multiple myeloma
  • combination therapy
  • drug induced