Transthyretin amyloid (ATTR) amyloidosis is an adult-onset, rare systemic disorder
characterized by the accumulation of misfolded fibrils in the body, including the peripheral …

ABSTRACT Introduction: Hereditary transthyretin amyloidosis (ATTRm amyloidosis) is a rare
disease caused by the deposition and accumulation of insoluble non-native transthyretin …

ABSTRACT Background & Aims: Hereditary transthyretin (ATTRv) amyloidosis represents a
diagnostic challenge considering the great variability in clinical presentation and multiorgan …

Transthyretin amyloidosis (ATTR) is a rare, progressive, life-threatening, hereditary disorder
caused by mutations in the transthyretin gene. Due to the phenotypic heterogeneity, ATTR is …

Gastrointestinal manifestations are common across all hereditary transthyretin amyloidosis
(ATTRv) genotypes. However, they are poorly specific, and their recognition as part of …

Purpose To review the management of gastrointestinal symptoms in patients with hereditary
transthyretin amyloidosis, discussing diagnostic evaluations, assessment of disease …

Hereditary transthyretin amyloidosis, once a rare progressive neuropathy and/or
cardiomyopathy, is now recognized with increasing worldwide frequency, various …

Hereditary Transthyretin Amyloidosis with Polyneuropathy: Monitoring and Management - PMC
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Amyloidoses represent a group of diseases characterized by the pathological accumulation
in the extracellular area of insoluble misfolded protein material called “amyloid”. The …

Background Hereditary transthyretin amyloidosis is an uncommon multisystem disorder
caused by mutation of the transthyretin protein, leading to peripheral neuropathy often with …