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Paroxysmal familial ventricular fibrillation

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Description

A rare, genetic, cardiac rhythm disease characterized by ventricular fibrillation in the absence of any structural or functional heart disease, or known repolarization abnormalities. The presence of J waves is associated with a higher risk of nocturnal ventricular fibrillation events and a higher risk of recurrence.

ORDO

  • Mode of Inheritance

    VARIANTS

    38

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    Genes

    External Links

    • OMIM
    • Orphanet

      228140

    • HPO
    • Medgen

      C0340493

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