Long QT syndrome with hearing impairment (Q66175)

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Jervell and Lange-Nielsen syndrome is an autosomal recessive variant of familial long QT syndrome characterised by congenital profound bilateral sensorineural hearing loss, a long QT interval on electrocardiogram and ventricular tachyarrhythmias.
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ID_1346057986
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    Long QT syndrome with hearing impairment
    Jervell and Lange-Nielsen syndrome is an autosomal recessive variant of familial long QT syndrome characterised by congenital profound bilateral sensorineural hearing loss, a long QT interval on electrocardiogram and ventricular tachyarrhythmias.

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      CID11:ID_1346057986
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      dki-india-ID_1346057986
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      Concluído
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      13 August 2026
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