… Therefore, dual organ heart/liver transplantation should be considered in patients with
familial transthyretin amyloidosis complicated by infiltrative cardiomyopathy [50]. The advent of …

… We review here the clinical features of cardiac ATTR amyloidosis and describe the diagnostic
tests to determine ATTR type. Correct diagnosis is ever more crucial given that several …

Hereditary transthyretin (ATTRv) amyloidosis is a rare and autosomal dominant disorder
associated with mutations in the transthyretin gene. Patients present with diverse symptoms …

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

… A key part of disease management for patients diagnosed with ATTRv amyloidosis includes
symptomatic treatments, which can reduce symptom burden but do not affect the underlying …

… Among the different types of amyloidosis, nearly all cases of clinical cardiac amyloidosis (>95%)
are caused by light chain amyloidosis (AL) and transthyretin amyloidosis (ATTR) [3,4]. …

… resulting in diagnostic delay. The field of amyloidosis has seen significant improvements
over the past decade in diagnostic accuracy, prognosis prediction and management. The …

… There are not many differences in the therapy of heart failure due to light-chain amyloid (AL)
and that of transthyretin amyloidosis (TTR). Diuretics form the mainstay of treatment in …

… diagnosis of stage 1 (patient is ambulatory) or stage 2 (patient is ambulatory with assistance)
hereditary transthyretin amyloidosis … besides hereditary transthyretin amyloidosis, previous …

… to describe clinical features, diagnostic tools, and … a diagnostic algorithm for identification
of cardiac amyloidosis. While treatment has historically focused on symptomatic management …