2014Muscle & NerveOpen access

Amyloid polyneuropathy caused by wild-type transthyretin

Lynda Lam, Marta Margeta, Robert B. Layzer

Open full text 19 citations

Abstract

INTRODUCTION: Amyloidosis derived from transthyretin (TTR) molecules is typically caused by mutations of the TTR gene. METHODS: We describe an elderly patient with a severe length-dependent polyneuropathy that unexpectedly proved to be caused by wild-type transthyretin amyloidosis. RESULTS: The diagnosis was made by muscle biopsy, because no amyloid deposits were found in the biopsied nerve segment. Most cases of wild-type transthyretin amyloidosis occur in elderly patients with cardiomyopathy, but a few cases of polyneuropathy have been reported. CONCLUSIONS: This entity is especially noteworthy in light of emerging treatment options for hereditary transthyretin amyloidosis, which are likely to also be beneficial in wild-type disease.

About this research paper

What this paper is about

INTRODUCTION: Amyloidosis derived from transthyretin (TTR) molecules is typically caused by mutations of the TTR gene. METHODS: We describe an elderly patient with a severe length-dependent polyneuropathy that unexpectedly proved to be caused by wild-type transthyretin amyloidosis. RESULTS: The diagnosis was made by muscle biopsy, because no amyloid deposits were found in the biopsied nerve segment. Most cases of wild-type transthyretin amyloidosis occur in elderly patients with cardiomyopathy, but a few cases of polyneuropathy have been reported. CONCLUSIONS: This entity is especially noteworthy in light of emerging treatment options for hereditary transthyretin amyloidosis, which are likely to also be beneficial in wild-type disease.

Why it matters

OpenAlex reports 19 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

INTRODUCTION: Amyloidosis derived from transthyretin (TTR) molecules is typically caused by mutations of the TTR gene. METHODS: We describe an elderly patient with a severe length-dependent polyneuropathy that unexpectedly proved to be caused by wild-type transthyretin amyloidosis. RESULTS: The diagnosis was made by muscle biopsy, because no amyloid deposits were found in the biopsied nerve segment. Most cases of wild-type transthyretin amyloidosis occur in elderly patients with cardiomyopathy, but a few cases of polyneuropathy have been reported. CONCLUSIONS: This entity is especially noteworthy in light of emerging treatment options for hereditary transthyretin amyloidosis, which are likely to also be beneficial in wild-type disease.

Key concepts: Transthyretin, Polyneuropathy, Amyloidosis, Medicine, Amyloid (mycology), Pathology, Cardiomyopathy, Amyloid polyneuropathy

Related papers

Back to paper searchBrowse research topicsOriginal source
Amyloid polyneuropathy caused by wild-type transthyretin — Research Paper | ScholarLens