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

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

Objective: Hereditary transthyretin amyloidosis (ATTRv) represents a diagnostic challenge
considering the great variability of clinical presentation and multiorgan involvement. In the …

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

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 …

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

Aims: In the current study we aimed to explore the prevalence of gastrointestinal (GI)
manifestations in hereditary transthyretin amyloid (hATTR) amyloidosis associated with …

Hereditary amyloidogenic transthyretin (ATTRv) amyloidosis is a rare autosomal dominantly
inherited disorder caused by mutations in the transthyretin (TTR) gene. The pathogenetic …

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

Background Despite emerging treatments for hereditary transthyretin (ATTRv) amyloidosis,
the disease is often misdiagnosed, with reported diagnostic delays of up to several years …