Results 41 to 50 of about 7,221 (188)
Thyrotoxic hypokalemic periodic paralysis [PDF]
QJM, 2016 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
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CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis
Clinical Case Reports, 2020 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
Acta Neuropathologica Communications, 2021 Hypokalemic periodic paralysis is an autosomal dominant, rare disorder caused by variants in the genes for voltage-gated calcium channel CaV1.1 (CACNA1S) and NaV1.4 (SCN4A).
Thomas O. Krag +3 more
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Hypokalemic Periodic Paralysis Precipitated by Thyrotoxicosis and Renal Tubular Acidosis
Case Reports in Endocrinology, 2021 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
Hypokalemic periodic paralysis
National Journal of Maxillofacial Surgery, 2012 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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An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene [PDF]
Korean Journal of Pediatrics, 2010 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
doaj +1 more source
Thyroid hypokalemic periodic paralysis
Journal of Osteopathic Medicine, 1998 Abstract An unusual presentation of thyrotoxicosis resulting in hypokalemic periodic paralysis is reported here. The patients with this disorder have very low serum potassium levels during the active phase of the disease. Very often, several months pass before the diagnosis is made.
M E, Nida, H, Kanj
openaire +2 more sources
Hypokalemic paralysis and acid-base balance
Emergency Care Journal, 2006 Three cases of hypokalemic paralysis are reported, presenting to the Emergency Department. The first is a patient with a hypokalemic periodic paralysis with a normal acid-base status, the second is a case of hypokalemic flaccid paralysis of all ...
Ivo Casagranda +4 more
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Thyrotoxic periodic paralysis: a case study and review of the literature
Journal of Community Hospital Internal Medicine Perspectives, 2017 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
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Levothyroxine and Prednisone Causing Generalized Weakness in a Middle-Aged Man
Case Reports in Endocrinology, 2012 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