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. 2008 Oct 21;1(1):256.
doi: 10.1186/1757-1626-1-256.

Hypokalemic Periodic Paralysis: a case report and review of the literature

Affiliations

Hypokalemic Periodic Paralysis: a case report and review of the literature

Benjamin R Soule et al. Cases J. .

Abstract

Hypokalemic Periodic Paralysis is one form of Periodic Paralysis, a rare group of disorders that can cause of sudden onset weakness. A case of a 29 year old male is presented here. The patient presented with sudden onset paralysis of his extremities. Laboratory evaluation revealed a markedly low potassium level. The patient's paralysis resolved upon repletion of his low potassium and he was discharged with no neurologic deficits. An association with thyroid disease is well established and further workup revealed Grave's disease in this patient. Although rare, Periodic Paralysis must differentiated from other causes of weakness and paralysis so that the proper treatment can be initiated quickly.

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Figures

Figure 1
Figure 1
Progression of EKG Findings. (A) The initial EKG revealed Mobitz Type I heart block. Several p-waves (solid arrows) are present that are not associated with a QRS complex. The duration of the PR interval continues to increase until a QRS is skipped (open arrow). (B) After treatment, the EKG revealed a return to a sinus rhythm.

References

    1. Fontaine B, Vale-Santos J, Jurkat-Rott K, Reboul J, Plassart E, Rime CS, Elbaz A, Heine R, Guimaraes J, Weissenbach J, et al. Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families. Nat Genet. 1994;6:267–272. doi: 10.1038/ng0394-267. - DOI - PubMed
    1. Jurkat-Rott K, Lerche H, Lehmann-Horn F. Skeletal muscle channelopathies. J Neurol. 2002;249:1493–1502. doi: 10.1007/s00415-002-0871-5. - DOI - PubMed
    1. Lin SH, Lin YF, Chen DT, Chu P, Hsu CW, Halperin ML. Laboratory tests to determine the cause of hypokalemia and paralysis. Arch Intern Med. 2004;164:1561–1566. doi: 10.1001/archinte.164.14.1561. - DOI - PubMed
    1. Kelley DE, Gharib H, Kennedy FP, Duda RJ, Jr, McManis PG. Thyrotoxic periodic paralysis. Report of 10 cases and review of electromyographic findings. Arch Intern Med. 1989;149:2597–2600. doi: 10.1001/archinte.149.11.2597. - DOI - PubMed
    1. Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G. Mutation screening in Chinese hypokalemic periodic paralysis patients. Mol Genet Metab. 2006;87:359–363. doi: 10.1016/j.ymgme.2005.10.020. - DOI - PubMed

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