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Published on: August 8, 2022
KLHL24-Associated Hypertrophic Cardiomyopathy: When Genotype Outpaces Phenotype.
Pramod Kumar1, Ahmad Ghayas Ansari1, Deepa Sasikumar1
1Department of Cardiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.
Kelch-like family member 24 (KLHL24)-associated hypertrophic cardiomyopathy (HCM) presents unique risks. Early genetic testing guides timely interventions like implantable cardioverter-defibrillator (ICD) placement, even in low-risk patients.
Area of Science:
- Cardiology
- Genetics
- Molecular Biology
Background:
- Kelch-like family member 24 (KLHL24)-associated hypertrophic cardiomyopathy (HCM) is a genetic disorder.
- Characterized by early onset and high risk of malignant ventricular arrhythmias.
- Caused by impaired cytoskeletal protein turnover.
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