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Neurological manifestations of hereditary transthyretin amyloidosis: a focus on diagnostic delays.

Michelle C KakuShivkumar BhadolaJohn L BerkVaishali SanchorawalaLawreen H ConnorsK H Vincent Lau
Published in: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis (2022)
Our study found higher rates of polyneuropathy by examination than patient-reported symptoms, especially among those with V122I TTR amyloidosis, signalling asymptomatic polyneuropathy. Our findings suggest the need for routine neurological examinations and other testing for genetic carriers to achieve earlier identification of active disease state.
Keyphrases
  • patient reported
  • multiple myeloma
  • genome wide
  • clinical practice
  • copy number
  • dna methylation
  • sleep quality
  • physical activity