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Cardiac fibroblast activation imaging in a patient with hypertrophic cardiomyopathy

Yu Zhang1, Yi-Lu Wang2, Min-Fu Yang1

  • 1Department of Nuclear Medicine, Beijing Chaoyang Hospital, Capital Medical University, 8th Gongtinanlu Road, Chaoyang District, Beijing, 100020, China.

Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology
|April 13, 2022
PubMed
Abstract

No abstract available in PubMed .

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Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

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75
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
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