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- W3156487374 abstract "Abstract Timothy Syndrome is a rare autosomal dominant multisystem genetic condition. The CACNA1C gene, codifier of the CaV1.2 calcium channel, is affected, resulting in the loss of voltage-dependent calcium channel inactivation. Relevant clinical characteristics: (1) corrected QT interval greater than 480ms; (2) syndactyly. Death often occurs during childhood, and results from ventricular tachyarrhythmias. This study presents the case of a female newborn who suffered a cardiorespiratory arrest, secondary to ventricular arrhythmia. A prolonged QT interval, combined with 2:1 AV block, [...]" @default.
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- W3156487374 date "2021-04-16" @default.
- W3156487374 modified "2023-10-16" @default.
- W3156487374 title "Aborted Sudden Death Due to Severe Ventricular Arrhythmia in Timothy Syndrome" @default.
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- W3156487374 doi "https://doi.org/10.36660/ijcs.20200061" @default.
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