Early diagnosis and management of patients with familial ATTR amyloidosis receiving livers from asymptomatic variant TTR carriers

Amyloid. 2011 Sep;18(3):172-3. doi: 10.3109/13506129.2011.594822. Epub 2011 Jul 21.

Abstract

The possibility of a patient with familial ATTR amyloidosis receiving a liver from an asymptomatic variant TTR carrier is remote [corrected].However, in 2008, it was reported that this unlikely event occurred in a patient in Portugal. We report our protocol for early diagnosis and management of this entity.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid Neuropathies, Familial / diagnosis
  • Amyloid Neuropathies, Familial / etiology
  • Amyloid Neuropathies, Familial / genetics
  • Amyloid Neuropathies, Familial / therapy
  • Amyloidosis, Familial / diagnosis*
  • Amyloidosis, Familial / etiology
  • Amyloidosis, Familial / genetics
  • Amyloidosis, Familial / therapy
  • Early Diagnosis
  • Humans
  • Liver / metabolism
  • Liver Transplantation*
  • Mutation
  • Prealbumin / genetics*
  • Prealbumin / metabolism

Substances

  • Prealbumin