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

Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies

1 May 2021

Abstract excerpt

Hypertrophic cardiomyopathy (HCM) and primary restrictive cardiomyopathy (RCM) have a similar genetic background as they are both caused mainly by variants in sarcomeric genes. These "sarcomeric cardiomyopathies" also share diastolic dysfunction as the prevalent pathophysiological mechanism. Starting from the observation that patients with HCM and primary RCM may coexist in the same family, a characteristic...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy and Myosin Studies
Share to Lysosomal Storage Disorders Research
Share to Trypanosoma species research and implications

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34062949
DOI: 10.3390/jcm10091954

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

Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and PhenocopiesPMID 34062949Read ↗

Genetics of hypertrophic and dilated cardiomyopathy.Semantic proximity Read ↗

Genetic Insights Into Primary Restrictive CardiomyopathySemantic proximity Read ↗

Hypertrophic Cardiomyopathies Phenocopies: Classification, Key Features and Differential DiagnosisSemantic proximity Read ↗

Hypertrophic cardiomyopathy: an introduction to pathology and pathogenesis.Semantic proximity Read ↗

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

Hypertrophic Cardiomyopathy: Genetic Foundations, Outcomes, Interconnections, and Their ModifiersSemantic proximity Read ↗

Hypertrophic CardiomyopathySemantic proximity Read ↗

Hypertrophic Cardiomyopathy: A ReviewSemantic proximity Read ↗

Hypertrophic cardiomyopathy: pathological features and molecular pathogenesis.Semantic proximity Read ↗

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.Semantic proximity Read ↗

Genetic Restrictive Cardiomyopathy: Causes and Consequences-An Integrative Approach.Semantic proximity Read ↗

[Hypertrophic cardiomyopathies].Semantic proximity Read ↗

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