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

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

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 …

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 …

Background Gastrointestinal (GI) complications are common in hereditary transthyretin
amyloidosis and an autonomic dysfunction has been considered to explain these symptoms …

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

Purpose Hereditary transthyretin amyloidosis (hATTR amyloidosis) is a progressive disease
primarily characterized by adult-onset sensory, motor, and autonomic neuropathy. In this …

Background Gastrointestinal complications are common in hereditary transthyretin amyloid
(ATTR m) amyloidosis. The underlying mechanisms have not been fully elucidated, and the …

Hereditary transthyretin amyloidosis is caused by pathogenic variants (ATTR v) in the TTR
gene. Alongside cardiac dysfunction, the disease typically manifests with a severely …