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A Rare Case of Hypokalemic Periodic Paralysis With Acute Urinary Retention: Diagnosis and Management. [PDF]
CureusSara S, Tv D, Dg G, Elumalai B, Javid M.
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Hypokalemic Periodic Paralysis Type 2 Due to SCN4A Val1105Met Mutation: A Case Study. [PDF]
CureusHu NQ, Yang JY, Lv JL, Zhu YZ, Li LH.
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Acetazolamide Prophylaxis in Hypokalemic Periodic Paralysis
New England Journal of Medicine, 1968Abstract When acetazolamide, an agent used to treat hyperkalemic periodic paralysis, was inadvertently found to relieve a patient with the hypokalemic variety, he and another patient were observed to compare this agent with conventional therapy. Well tolerated doses of acetazolamide, 375 to 500 mg daily, eliminated severe attacks and were much more ...
Griggs Robert C +2 more
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Hypokalemic Periodic Paralysis
Consultant, 2023Abstract The review chapter on hypokalemic periodic paralysis (HypoPP) examines the epidemiology, genetic basis, and pathophysiology of this rare hereditary channelopathy. It discusses diagnostic considerations, prevention, and treatment options, including the role of acetazolamide.
Brett Simmons, David Matteson
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Hypokalemic Periodic Paralysis
Southern Medical Journal, 1984Hypokalemic periodic paralysis is an unusual disease that may begin dramatically. Although terrifying to the patient, the attacks can usually be controlled if the proper diagnosis is made. Although much has been done to determine the pathogenesis, many questions remain unanswered.
V, Johnson, W W, Winternitz
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