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

Identification of a Novel Genetic Locus for Familial Cardiac Myxomas and Carney Complex

8 Dec 1998

Abstract excerpt

BACKGROUND: Intracardiac myxomas are significant causes of cardiovascular morbidity and mortality through embolic stroke and heart failure. In the autosomal dominant syndrome Carney complex, intracardiac myxomas arise in the setting of lentiginosis and other lesions associated with cutaneous hyperpigmentation, extracardiac myxomas, and nonmyxomatous tumors. Genetic factors that regulate cardiac tumor growth...

Read the complete abstract on PubMed

Topics

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

Share to Cardiac tumors and thrombi
Share to Coronary Artery Anomalies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9843463
DOI: 10.1161/01.cir.98.23.2560

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a Novel Genetic Locus for Familial Cardiac Myxomas and Carney ComplexPMID 9843463Read ↗

Molecular genetic diagnosis of the familial myxoma syndrome (Carney complex).Semantic proximity Read ↗

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.Semantic proximity Read ↗

Molecular features, markers, drug targets, and prospective targeted therapeutics in cardiac myxoma.Semantic proximity Read ↗

Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q.Semantic proximity Read ↗

Recurrent left atrial myxomas in Carney complex: a genetic cause of multiple strokes that can be prevented.Semantic proximity Read ↗

Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).Semantic proximity Read ↗

Medical and Surgical Management of Carney Complex.Semantic proximity Read ↗

Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complexSemantic proximity Read ↗

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27Semantic proximity Read ↗

Severe tortuosity and stenosis of the systemic, pulmonary and coronary vessels in 12 patients with similar phenotypic features: a new syndrome?Semantic proximity Read ↗

Fatal Carney Complex in Siblings Due to De Novo Large Gene Deletion.Semantic proximity Read ↗

Genetic testing of the family with a Carney-complex member leads to successful early removal of an asymptomatic atrial myxoma in the mother of the patient.Semantic proximity Read ↗

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