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Family screening of hypertrophic cardiomyopathy in children: a case report
BACKGROUND: Paediatric hypertrophic cardiomyopathy (HCM) caused by sarcomere protein gene mutations is more common than previously thought. We present the case of a 9-year-old boy that was diagnosed with HCM during family screening. CASE SUMMARY: We present a case of a 9-year-old boy with a family h...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477208/ https://www.ncbi.nlm.nih.gov/pubmed/36128439 http://dx.doi.org/10.1093/ehjcr/ytac360 |