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Article

Morphological and Genetic Aspects for Post-Mortem Diagnosis of Hypertrophic Cardiomyopathy: A Systematic Review.

International journal of molecular sciences - 20 Jan 2024

Cianci Vincenzo, Forzese Elena, Sapienza Daniela, Cardia Luigi, Cianci Alessio, Germanà Antonino, Tornese Lorenzo, Ieni Antonio, Gualniera Patrizia, Asmundo Alessio, Mondello Cristina

Abstract excerpt

Hypertrophic cardiomyopathy (HCM) is one of the most common genetic cardiovascular diseases, and it shows an autosomal dominant pattern of inheritance. HCM can be clinically silent, and sudden unexpected death due to malignant arrhythmias may be the first manifestation. Thus, the HCM diagnosis could be performed at a clinical and judicial autopsy and offer useful findings on morphological features; moreover, it...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 38279275
DOI: 10.3390/ijms25021275
PMCID: PMC10816624

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.

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