Long-term follow-up of a patient with type 2 Timothy syndrome and the partial efficacy of mexiletine - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Gene Année : 2021

Long-term follow-up of a patient with type 2 Timothy syndrome and the partial efficacy of mexiletine

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Résumé

We report a detailed case of type 2 TS due to a p.(Gly402Ser) mutation in exon 8 of the CACNA1C gene. The patient shows a marked prolongation of repolarization with a mean QTc of 540 ms. He shows no structural heart disease, syndactyly, or cranio-facial abnormalities. However, he shows developmental delays, without autism, and dental abnormalities. The cardiac phenotype is very severe, with a resuscitated cardiac arrest at 2.5 years of age, followed by 26 appropriate shocks during nine years of follow-up. Adding mexiletine to nadolol resulted in a reduction of the QTc and a slight decrease in the number of appropriate shocks.

Dates et versions

hal-03564793 , version 1 (10-02-2022)

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Citer

Alexis Hermida, Guillaume Jedraszak, Maciej Kubala, Amel Mathiron, Pascal Berna, et al.. Long-term follow-up of a patient with type 2 Timothy syndrome and the partial efficacy of mexiletine. Gene, 2021, 777, ⟨10.1016/j.gene.2021.145465⟩. ⟨hal-03564793⟩

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