The researchers found that MYH7, MYBPC3, and TTN mutations were the most common mutations (71%) found in genetic NCCM. HealthDay News — Genetic stratification should play a role in clinical care of ...
Non-compaction cardiomyopathy is a heart condition caused by defects that arise during fetal development and can have diverse health impacts in affected individuals, including sudden cardiac death.
Non-compaction cardiomyopathy is a heart condition caused by defects that arise during fetal development and can have diverse health impacts in affected individuals, including sudden cardiac death.
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Genetics of cardiomyopathy risk in childhood cancer survivors differ by age of onset, study shows
The relationship between genetic variants and the risk of late-onset cardiomyopathy remains poorly understood in survivors of childhood cancer despite being otherwise well established. Scientists from ...
BUFFALO, N.Y. — A national, University at Buffalo-led study on genes in pediatric cardiomyopathy demonstrates strong evidence for routine genetic screening in children with the disease. The study, ...
MINNEAPOLIS — By definition, a variant of unknown significance identified in an individual with cardiomyopathy can leave physicians wondering what to do with the information. Don’t discard so-called ...
Hypertrophic cardiomyopathy (HCM) is the most common genetic heart (cardiac) condition. It affects more than one in 500 people in the US. Genetic counseling and genetic testing can be helpful so you ...
Hypertrophic cardiomyopathy (HCM) is a genetic heart condition that can potentially cause serious complications. The condition runs in families, so if youve been diagnosed, you may have concerns about ...
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