ArticleAME case reports2026
Hypertrophic cardiomyopathy associate with a
Article in AME case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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4 authors.
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Abstract
Background: Hypertrophic cardiomyopathy (HCM) is a common hereditary disease of the myocardium, caused by mutations in at least 20 genes, encoding cardiac sarcomere proteins and sarcomere-associated proteins, while genes related to calcium metabolism, such as phospholamban ( Case Description: A 13-year-old male patient was admitted to the hospital due to "skin pallor", and was diagnosed with mild thalassemia by cytopenia and loss of heterozygosity of thalassemia gene α3.7. The symptoms were improved after iron supplementation. During hospitalization, the child complained of precordial pain. Echocardiogram and cardiac magnetic resonance (CMR) were performed, which showed thickening of the anterior septal basal segment, with the maximum thickness of 14 mm and a Z-score of 5.6 (Boston standard), and left ventricular outflow tract obstruction (dynamic). The subject carried a missense mutation of Conclusions: This case highlights HCM caused by
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