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
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
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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
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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 Precipitated by Thyrotoxicosis and Renal Tubular Acidosis
Background. Hypokalemic periodic paralysis is a rare neuromuscular disorder characterized by transient episodes of flaccid paralysis due to a defect in muscle ion channels. Most cases are hereditary, but it can be acquired.
Ian Jackson +9 more
doaj +1 more source
Thyrotoxic periodic paralysis: a case study and review of the literature
Acute hypokalemic paralysis is a rare cause of acute weakness. Morbidity and mortality associated with unrecognized disease can occur and include respiratory failure and possibly death.
Marcelle Meseeha +3 more
doaj +1 more source
Levothyroxine and Prednisone Causing Generalized Weakness in a Middle-Aged Man
Thyrotoxic induced hypokalemic periodic paralysis is a rare disorder that had been described in middle-aged men, predominantly Asians and Hispanics.
Andrew Word +2 more
doaj +1 more source
An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene [PDF]
Familial hypokalemic periodic paralysis is an autosomal-dominant channelopathy characterized by episodic muscle weakness with hypokalemia. The respiratory and cardiac muscles typically remain unaffected, but we report an atypical case of a family with ...
Yang Hee Park, June Bum Kim
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A Case of Hypokalemic Periodic Paralysis in a Young Athlete.
Hypokalemic periodic paralysis (HPP) is one of the group muscle disorders that can cause sudden onset paresis or paralysis. It is a quite rare, yet, potentially life-threatening condition that, if appropriately and promptly diagnosed and treated, can be ...
Nasser, Hesham +3 more
core +1 more source
Reversible electrophysiological abnormalities in hypokalemic paralysis: Case report of two cases
Compound muscle action potential (CMAP) amplitude declines during a paralytic attack in patients with hypokalemic periodic paralysis (HPP). However, serial motor nerve conduction studies in hypokalemic paralysis have not been commonly reported. We report
C M Sharma, Kunal Nath, Jigar Parekh
doaj +1 more source

