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February 1965

Periodic Paralysis in Taiwan: Clinical Study of 28 Cases

Author Affiliations

From the Department of Neurology and Psychiatry, National Taiwan University Hospital, Taipei, Taiwan, Republic of China.

Arch Neurol. 1965;12(2):165-171. doi:10.1001/archneur.1965.00460260055007

Introduction  THE PURPOSE of this report is to describe the characteristic features of periodic paralysis as it is seen among the Chinese on Taiwan. This disease, contrary to previous publications, has been found to be not uncommon in this area.It has now been well recognized that a number of different etiologic factors and metabolic disturbances may produce a clinical syndrome of periodic paralysis of the nonfamilial type. Furthermore, it would appear that the dominant heredofamilial type is relatively uncommon.1-5In general, potassium metabolism has been implicated and cases of sporadic hypokalemic periodic paralysis have been reported as a result of potassium-losing nephritis,6 primary or intermittent aldosteronism,7,8 and other causes for potassium deficiency.9 There have also been instances of periodic paralysis reported in which the serum potassium levels have been found to be normal.5,10,11 Hyperkalemic paralysis or adynamia episodica hereditaria has also been

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