Considering the rare incidence of transthyretin amyloidosis cardiomyopathy (ATTR-CM) in
Poland, patients encounter difficulties at the stages of diagnosis and treatment. For …

We aimed to ascertain whether sex-related differences are relevant to clinical presentation,
cardiac phenotype and all-cause mortality in different types of cardiac amyloidosis, a field …

Abstract Background The p. Glu109Lys variant (Glu89Lys) is a rare cause of hereditary
transthyretin amyloidosis (ATTRv) for which clinical spectrum remains unresolved. We …

Amyloid cardiomyopathy (CA) was previously considered a rare disease; however, rapid
advancements in imaging modalities have led to an increased frequency of its diagnosis …

Aims We conducted a presentation on an 84‐year‐old male patient who has been
diagnosed with TTRA81V (p. TTRA101V) hereditary transthyretin cardiac amyloidosis …

Background and Objectives: Hereditary transthyretin amyloidosis (ATTRv) is a rare disease
caused by pathogenic variants in the transthyretin (TTR) gene. More than 140 different …

Amyloid transthyretin cardiomyopathy is a progressive disease that confers significant
mortality. While it is relatively rare, the frequency of diagnoses has risen with the increased …

A 64 years-old woman with intestinal neuroendocrine tumor (NET) and multiple liver
metastases was referred for peptide receptor radioligand therapy (PRRT) with [177Lu] Lu …

Z uwagi na rzadkie występowanie w Polsce amyloidozy transtyretynowej serca (ATTR-CM,
transthyretin amyloidosis cardiomyopathy) pacjenci napotykają na liczne trudności na etapie …

Hereditary transthyretin amyloidosis (hATTR) is a progressive, autosomal dominant,
multisystem disease with incomplete and age-related penetrance. The disease presents …