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  2. Brugada syndrome - Wikipedia

    en.wikipedia.org/wiki/Brugada_syndrome

    Brugada syndrome was described as a cause for the sudden unexplained cardiac death syndrome seen in Thai men in 1997. [50] The first genetic mutations affecting the SCN5A gene associated with the syndrome were identified by their brother Ramon Brugada in 1998, [ 13 ] with many more mutations affecting at least 19 genes subsequently identified ...

  3. List of human disease case fatality rates - Wikipedia

    en.wikipedia.org/wiki/List_of_human_disease_case...

    Human infectious diseases may be characterized by their case fatality rate (CFR), the proportion of people diagnosed with a disease who die from it (cf. mortality rate).It should not be confused with the infection fatality rate (IFR), the estimated proportion of people infected by a disease-causing agent, including asymptomatic and undiagnosed infections, who die from the disease.

  4. Ajmaline - Wikipedia

    en.wikipedia.org/wiki/Ajmaline

    Brugada syndrome is a genetic disease that can result in mutations in the sodium ion channel (gene SCN5A) of the myocytes in the heart. [10] Brugada syndrome can result in ventricular fibrillation and potentially death. It is a major cause of sudden unexpected cardiac death in young, otherwise healthy people. [11]

  5. Sudden unexplained nocturnal death syndrome - Wikipedia

    en.wikipedia.org/wiki/Sudden_unexplained...

    Sudden unexplained nocturnal death syndrome may refer to: Brugada syndrome , a genetic disorder in which the electrical activity within the heart is abnormal Sudden arrhythmic death syndrome (SADS), a sudden unexpected death of adolescents and adults, mainly during sleep

  6. Sudden arrhythmic death syndrome - Wikipedia

    en.wikipedia.org/wiki/Sudden_arrhythmic_death...

    Sudden death of a young person can be caused by heart disease (including cardiomyopathy, congenital heart disease, myocarditis, genetic connective tissue disorders) or conduction disease (WPW syndrome, etc.), medication-related causes or other causes. [13]

  7. Channelopathy - Wikipedia

    en.wikipedia.org/wiki/Channelopathy

    Long QT syndrome, the most common form of cardiac channelopathy, is characterized by prolonged ventricular repolarization, predisposing to a high risk of ventricular tachyarrhythmias (e.g., torsade de pointes), syncope, and sudden cardiac death.

  8. Case fatality rate - Wikipedia

    en.wikipedia.org/wiki/Case_fatality_rate

    They are neither rates, incidence rates, nor ratios (none of which are limited to the range 0–1). They do not take into account time from disease onset to death. [4] [5] Sometimes the term case fatality ratio is used interchangeably with case fatality rate, but they are not the same. A case fatality ratio is a comparison between two different ...

  9. List of ICD-9 codes 740–759: congenital anomalies - Wikipedia

    en.wikipedia.org/wiki/List_of_ICD-9_codes_740...

    758.0 Down syndrome; 758.1 Patau's syndrome; 758.2 Edward's syndrome; 758.3 Autosomal deletion syndromes 758.31 Cri du chat syndrome; 758.32 Velo-cardio-facial syndrome; 758.33 Other microdeletions. Miller–Dieker syndrome; Smith–Magenis syndrome; 758.4 Balanced autosomal translocation in normal individual; 758.5 Other conditions due to ...