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Case report details periodic paralysis in Andersen–Tawil syndrome, suggesting comparisons to myotonica congenita.
Background/Purpose: Andersen–Tawil-syndrome (ATS) is a distinct potassium channelopathy. Due to its rarity (1:500,000), establishment of evidence based therapeutic interventions is challenging. Treatment guidance in ATS, therefore, is mainly on individual basis. The aim of this presentation was to improve the knowledge on treatment of periodic paralysis in ATS.
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Küpper et al. (2025) studied this question.
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