Key result
Molecular genetic testing enables personalized care in a young patient with two inherited arrhythmic syndromes.
Why the study?
Molecular genetic testing can influence treatment, risk assessment, and identification of at-risk family members in inherited arrhythmic syndromes, supporting personalized medicine.
Case Report (n=1)
Genetic testing can play a crucial role in the personalized management of patients with complex inherited arrhythmic syndromes.
The results of molecular genetic testing may affect recommended treatment or therapeutic decisions and risk assessment, may help with identification of family members at risk. Here, we report a case of a young patient with a paradoxical combination of two inherited arrhythmic syndromes and demonstrate the role of genetic testing as one of the basis of personalized approach in diagnosis, treatment and prevention complications of inherited channelopathies complications. Integration of genetic testing results into clinical practice is a successful example of the concept of personalized medicine.
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Блохина et al. (2022) conducted a case report in Inherited arrhythmic syndromes (n=1). Genetic testing was evaluated. Molecular genetic testing in a young patient with two inherited arrhythmic syndromes facilitated a personalized approach to diagnosis, treatment, and prevention of complications.
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