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

A case of premature and recurrent myocardial infarction associated with ABCA.1 gene mutation.

Journal of postgraduate medicine - 1 Jan 2000

Subramaniam K, Babu L A, Shah N

Abstract excerpt

Coronary heart disease (CHD) is the most important cause of cardiovascular death and when premature, it affects the most productive population of the community. Premature CHD usually has a specific etiology, which on diagnosis, might help in the secondary prevention in that individual. We report a case of young adult with recurrent myocardial infarction, who on evaluation had mildly reduced HDL and Protein C...

Read the complete abstract on PubMed

Topics

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

Share to ATP Binding Cassette Transporter 1
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myocardial Infarction

Share to Tangier Disease

Source

Open in PubMed Open full text

Identifiers

PMID: 33380594
DOI: 10.4103/jpgm.JPGM_70_20
PMCID: PMC8098876

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

A case of premature and recurrent myocardial infarction associated with ABCA.1 gene mutation.PMID 33380594Read ↗

A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large familySemantic proximity Read ↗

Tangier disease: still more questions than answers.Semantic proximity Read ↗

Three novel ATG16L1 mutations in a patient with acute myocardial infarction and coronary artery ectasia: A case report.Semantic proximity Read ↗

Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.Semantic proximity Read ↗

A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.Semantic proximity Read ↗

Variations on a gene: rare and common variants in ABCA1 and their impact on HDL cholesterol levels and atherosclerosis.Semantic proximity Read ↗

Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency.Semantic proximity Read ↗

Double Trouble-Hyperhomocysteinemia and Lipoprotein(a) Induced Myocardial Infarction in Very Young - A Case ReportSemantic proximity Read ↗

A novel variant in the ABCA1 gene for Tangier Disease with diffuse histiocytosis of bone marrow.Semantic proximity Read ↗

Effect of ABCA1 mutations on risk for myocardial infarction.Semantic proximity Read ↗

Coronary heart disease in a patient with cerebrotendinous xanthomatosis.Semantic proximity Read ↗

Myocardial infarction in a 36-year-old man with combined ABCA1 and APOA-1 deficiency.Semantic proximity Read ↗

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