Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Familial amyloid cardiomyopathy masquerading as chronic Guillain-Barre syndrome: things are not always what they seem.

Frontiers of medicine - 1 Jun 2017

Hu Die, Liu Ling, Yuan Shuguang, Yi Yuhong, Peng Daoquan

Abstract excerpt

Familial amyloid cardiomyopathy is a challenging condition that mimics many other diseases, particularly in patients with pronounced neurological presentations and unexplained or equivocal cardiac abnormalities. In this case, a 57-year-old man was admitted for outpatient cardiological evaluation of progressive right heart failure and limb paraesthesias. The patient presented with hypertension, chronic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyloid
Share to Amyloidosis, Familial
Share to Echocardiography, Doppler

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrocardiography, Ambulatory

Share to Guillain-Barre Syndrome

Share to Heart Ventricles

Share to Prealbumin

Share to Sick Sinus Syndrome

Source

Identifiers

PMID: 28425041
DOI: 10.1007/s11684-017-0516-9

Genes

TTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial amyloid cardiomyopathy masquerading as chronic Guillain-Barre syndrome: things are not always what they seem.PMID 28425041Read ↗

Transthyretin amyloidosis: an under-recognized neuropathy and cardiomyopathySemantic proximity Read ↗

Cardiac amyloidosis: An update on pathophysiology, diagnosis, and treatment.Semantic proximity Read ↗

Cardiac amyloidosis: when to suspect and how to confirm.Semantic proximity Read ↗

Cardiac amyloidosis: the great pretender.Semantic proximity Read ↗

ATTR Epidemiology, Genetics, and Prognostic FactorsSemantic proximity Read ↗

Amyloid Cardiomyopathy.Semantic proximity Read ↗

A novel TTR mutation (p.Ala65Val) underlying late-onset hereditary transthyretin (ATTRv) amyloidosis with mixed cardiac and neuropathic phenotype: a case report.Semantic proximity Read ↗

Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association.Semantic proximity Read ↗

Transthyretin-related amyloidoses and the heart: a clinical overview.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis: a case report.Semantic proximity Read ↗

A Case of Early Hereditary Transthyretin Amyloid Cardiomyopathy Recognition With Genetic Screening: A Case Report.Semantic proximity Read ↗

Unusual presentation of rare Phe33Leu mutation in hereditary TTR cardiac amyloidosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.