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Clinical characteristics and etiology-specific outcome in pediatric hypertrophic cardiomyopathy

Childhood-onset cardiomyopathies are rare disease (incidence 1/100,000) presenting with diverse, potentially severe phenotypes. The etiologies range from idiopathic/sarcomeric forms to syndromic diseases, neuromuscular disorders, and inborn errors of metabolism, but cause-specific outcomes remain in...

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Main Authors: Minette, Felix (Author) , Klass, Maximilian (Author) , Meyer, Nikita (Author) , Merzweiler, Angela (Author) , Burkart, Sebastian (Author) , Hempel, Maja (Author) , Frey, Norbert (Author) , Völkers, Mirko (Author) , Gorenflo, Matthias (Author) , Kovacevic, Alexander (Author) , Sandmann, Christoph (Author)
Format: Article (Journal)
Language:English
Published: 2025
In: Clinical research in cardiology
Year: 2025, Pages: 1-16
ISSN:1861-0692
DOI:10.1007/s00392-025-02703-7
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1007/s00392-025-02703-7
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Author Notes:Felix Minette, Maximilian Klass, Nikita Meyer, Angela Merzweiler, Sebastian Burkart, Maja Hempel, Norbert Frey, Mirko Völkers, Matthias Gorenflo, Alexander Kovacevic, Christoph Sandmann
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Summary:Childhood-onset cardiomyopathies are rare disease (incidence 1/100,000) presenting with diverse, potentially severe phenotypes. The etiologies range from idiopathic/sarcomeric forms to syndromic diseases, neuromuscular disorders, and inborn errors of metabolism, but cause-specific outcomes remain incompletely understood. This study analyzed the clinical course of a large cohort of children with hypertrophic cardiomyopathy (HCM), stratified by etiology.
Item Description:Publikationsdatum: 13. Oktober 2025 (online)
Gesehen am 07.04.2026
Physical Description:Online Resource
ISSN:1861-0692
DOI:10.1007/s00392-025-02703-7

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