Reversible Severe Rhabdomyolysis Associated with Thyrotoxic Hypokalemic Periodic Paralysis
- PMID: 34248576
- PMCID: PMC8255658
- DOI: 10.1159/000516771
Reversible Severe Rhabdomyolysis Associated with Thyrotoxic Hypokalemic Periodic Paralysis
Abstract
We report a case of reversible symptomatic rhabdomyolysis associated with thyrotoxic hypokalemic periodic paralysis. The patient had neither past medical nor family history of either disorder. The presenting neurological symptoms and signs, serum potassium, and creatine kinase levels returned to normal without specific treatment. Based on previous case reports, we attributed the combination of the disorders to a mutation of the calcium-gated channel (CACN) gene and its related encoded proteins.
Keywords: Electrolytes; Endocrine gland; Ion channel gene; Rhabdomyolysis.
Copyright © 2021 by S. Karger AG, Basel.
Conflict of interest statement
The authors declare that they have no conflicts of interest to disclose.
References
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- Anandan C, Cipriani MA, Laughlin RS, Niu Z, Milone M. Rhabdomyolysis and fluctuating asymptomatic hyperCKemia associated with CACNA1S variant. Eur J Neurol. 2018 Feb;25((2)):417–9. - PubMed
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