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

Cardiac Anderson-Fabry disease: lessons from a 25-year-follow up.

Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology - 1 Apr 2014

Brito Dulce, Miltenberger-Miltenyi Gabriel, Moldovan Oana, Navarro Carmen, Madeira Hugo Costa

Abstract excerpt

Sarcomeric hypertrophic cardiomyopathy (HCM) is the most common genetic cause of unexplained left ventricular hypertrophy and has no specific treatment. Anderson-Fabry disease (AFD) is rare and usually multisystemic, but occasionally expresses clinically as a predominantly cardiac phenotype mimicking HCM. We describe an illustrative case of a patient followed regularly for 25 years with a diagnosis of familial...

Read the complete abstract on PubMed

Topics

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

Share to Fabry Disease
Share to Follow-Up Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to GLA gene

Share to Heart Diseases

Share to Mutation

Share to Pedigree

Share to Time Factors

Source

Identifiers

PMID: 24830310
DOI: 10.1016/j.repc.2013.10.014

Genes

GLA

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

Cardiac Anderson-Fabry disease: lessons from a 25-year-follow up.PMID 24830310Read ↗

Diagnostic clues for the diagnosis of nonsarcomeric hypertrophic cardiomyopathy (Phenocopies): Amyloidosis, fabry disease, and mitochondrial diseaseSemantic proximity Read ↗

Prevalence of Anderson-Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson-Fabry Disease survey.Semantic proximity Read ↗

Anderson-Fabry disease: a rare phenocopy of hypertrophic cardiomyopathy.Semantic proximity Read ↗

Different Phenotypes of Anderson-Fabry Disease Identified with Cardiac Magnetic Resonance Imaging in a Family with the Same Late-Onset Mutation.Semantic proximity Read ↗

Fabry disease cardiomyopathy: A state-of-the-art review.Semantic proximity Read ↗

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy.Semantic proximity Read ↗

Clinical spectrum, cardiac phenotypes, and outcomes of FHL1-related cardiomyopathies: a systematic review.Semantic proximity Read ↗

Fabry disease: A fundamental genetic modifier of cardiac function.Semantic proximity Read ↗

Clinical and genetic spectrum in Chinese families with Fabry disease: a single-centre case series.Semantic proximity Read ↗

Identification of Fabry Disease in a Tertiary Referral Cohort of Patients with Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women.Semantic proximity Read ↗

Cardiac abnormalities in Anderson-Fabry disease and Fabry's cardiomyopathy.Semantic proximity Read ↗

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