MAIN ASPECTS OF BRUGADA SYNDROME
To date, there is a sufficient amount of data on the nature of diseases associated with the risk of sudden death. It is shown that many of them are genetically determined, and this is particularly dangerous, since not only the patient who has been diagnosed with the disease, but also his children an...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
InterMedservice
2020-03-01
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| Series: | Евразийский Кардиологический Журнал |
| Subjects: | |
| Online Access: | https://www.heartj.asia/jour/article/view/5391 |
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| Summary: | To date, there is a sufficient amount of data on the nature of diseases associated with the risk of sudden death. It is shown that many of them are genetically determined, and this is particularly dangerous, since not only the patient who has been diagnosed with the disease, but also his children and close relatives are at risk. Such diseases are rarely detected in normal clinical practice, and patients die, as a rule, not in specialized hospitals, but at home or on the street, and the doctor of the polyclinic or the ambulance crew remains to state the death. Cardiologists often pay attention only to the first symptoms of the disease, primarily syncope and palpitations, but also often the first and last manifestation of the disease is sudden death. Modern clinical medicine identifies a number of diseases and syndromes that are closely associated with a high risk of sudden death at a young age. These include one of the most «mysterious» diseases — Brugada syndrome (SB). |
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| ISSN: | 2225-1685 2305-0748 |