نتایج جستجو برای: hypokalemic paralysis

تعداد نتایج: 20271  

Journal: :The Journal of the Association of Physicians of India 1996
N Thomas B Ramakrishna M S Seshadri

periodic paralysis is a rare disorder characterized by transient attacks of flac-cid paralysis of varying intensity and frequency. Although mostly familial in etiology, several sporadic cases with different causes have been reported, including some resulting from renal tubular acidosis. 1 This article reports the case of a young man with secondary hypokalemic periodic paralysis caused by distal...

Journal: :acta medica iranica 0
m. h. harirchian m. ghaffarpour m. h. shahbazi

primary hypokalemic periodic paralysis is a familial channelopathy inherited as an autosomal dominant trait. the first attack of paralysis may be evolved at any age, but has been reported to be most common in the second decade, so that some authorities believe that an episodic weakness beginning after age 25 is almost never due to primary periodic paralysis. in this retrospective study, we revi...

Journal: :JAMA neurology 2013
Renrong Yang Karin Jurkat-Rott Jinlin Cao Guofeng Wang Hans-Peter Seelig Changping Yang Guibao Liu Lin Pan Haiyan Zheng Frank Lehmann-Horn

IMPORTANCE Hypokalemic periodic paralysis is a muscle channelopathy based on mutations or predisposing variants or secondary to potassium wasting. In contrast to myasthenia gravis, an association with thymic hyperplasia has not yet been reported, to our knowledge. OBSERVATIONS We report a male patient in his mid-20s with progressive episodes of flaccid muscle weakness, associated low serum po...

2013
Hong Ki Min Eun Oh Kim Sang Ju Lee Yoon Kyung Chang Kwang Sun Suh Chul Woo Yang Suk Young Kim Hyeon Seok Hwang

BACKGROUND Rifampin is one of the most important drugs in first-line therapies for tuberculosis. The renal toxicity of rifampin has been reported sporadically and acute tubulointerstitial nephritis (ATIN) is a frequent histological finding. We describe for the first time a case of ATIN and Fanconi syndrome presenting as hypokalemic paralysis, associated with the use of rifampin. CASE PRESENTA...

Journal: :Neurology 2004
T M Miller M R Dias da Silva H A Miller H Kwiecinski J R Mendell R Tawil P McManis R C Griggs C Angelini S Servidei J Petajan M C Dalakas L P W Ranum Y H Fu L J Ptácek

BACKGROUND Periodic paralyses and paramyotonia congenita are rare disorders causing disabling weakness and myotonia. Mutations in sodium, calcium, and potassium channels have been recognized as causing disease. OBJECTIVE To analyze the clinical phenotype of patients with and without discernible genotype and to identify other mutations in ion channel genes associated with disease. METHODS Th...

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