The role of nephrologists in management of hypokalemic periodic paralysis: a case report
Background Hypokalemic periodic paralysis is a chronic condition characterized by sporadic attacks of weakness associated with acute hypokalemia. Attacks are typically associated with specific triggers, such as prolonged rest following exercise or ...
Julia Li, Suha Moten, Anis A. Rauf
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Thyrotoxic Hypokalemic Periodic Paralysis: A Case Report
Thyrotoxic hypokalemic periodic paralysis is a rare and fatal complication of hyperthyroidism and is associated with low serum potassium levels and muscle weakness. Herein, we presented a young male patient who did not use the antithyroid drugs given for
Şeyma Esenbuğa +2 more
doaj +1 more source
Enhancement of K+ conductance improves in vitro the contraction force of skeletal muscle in hypokalemic periodic paralysis [PDF]
An abnormal ratio between Na+ and K+ conductances seems to be the cause for the depolarization and paralysis of skeletal muscle in primary hypokalemic periodic paralysis.
Quasthoff, Stefan +7 more
core +1 more source
Hypokalemic periodic paralysis
Hypokalemic periodic paralysis is a rare genetic disorder characterized by recurrent attacks of skeletal muscle weakness with associated hypokalemia which is precipitated by stress, cold, carbohydrate load, infection, glucose infusion, hypothermia, metabolic alkalosis, anesthesia, and steroids.
Abbas, Haider +2 more
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Thyrotoxic hypokalemic periodic paralysis [PDF]
Learning points for clinicians Non-selective beta-blockers, avoidance of high-salt, carbohydrate-rich meals and strenuous exertion are essential in acute management, until thyrotoxicosis is treated. Unlike primary, or familial, hypokalemic periodic paralysis, potassium supplementation alone is ineffective.1 Acetazolamide and T4 supplementation may ...
A, Zayac +5 more
openaire +2 more sources
Hypokalemic Periodic Paralysis in a Young Woman With Mast Cell Activation Syndrome: A Case Report of an Atypical Presentation Associated With an Ultra-Rare CACNA1S Variant. [PDF]
ABSTRACT Hypokalemic periodic paralysis (hKPP) is a rare neuromuscular channelopathy characterized by transient episodes of muscle weakness or paralysis associated with low serum potassium levels. It has been most commonly linked to autosomal dominant mutations in ion channel genes, specifically CACNA1S and SCN4A, which impair skeletal muscle ...
Moradi A +8 more
europepmc +2 more sources
CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis
It has long been believed that the patients with thyrotoxic hypokalemic periodic paralysis (THPP) may harbor genetic mutations commonly found in familial hypokalemic periodic paralysis.
Nader Rezkalla +5 more
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Perioperative Management of Hypokalemic Periodic Paralysis
A 64-year-old female presented for right ankle hardware removal. The patient’s daughter had recently been diagnosed with symptomatic hypokalemic periodic paralysis, and while our patient was asymptomatic, she was currently undergoing testing and thus was
Bolz, Erica +2 more
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Hypokalemic Periodic Paralysis Secondary to Thyrotoxicosis [PDF]
Background: Hypokalemic Periodic Paralysis (HPP) is a rare neuromuscular disorder characterized by acute, transient muscle weakness and paralysis secondary to hypokalemia and can be complicated by cardiac arrhythmias.
Kutty, Anugraha +3 more
core +1 more source
Clinical and biochemical spectrum of hypokalemic paralysis in North: East India
Background: Acute hypokalemic paralysis, characterized by acute flaccid paralysis is primarily a calcium channelopathy, but secondary causes like renal tubular acidosis (RTA), thyrotoxic periodic paralysis (TPP), primary hyperaldosteronism, Gitelman′s ...
Ashok K Kayal +3 more
doaj +1 more source

