Please use this identifier to cite or link to this item: http://adhlui.com.ui.edu.ng/jspui/handle/123456789/3065
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dc.contributor.authorBILLINGHURST, J R-
dc.contributor.authorJ AGWE, J G M-
dc.date.accessioned2024-10-10T12:35:58Z-
dc.date.available2024-10-10T12:35:58Z-
dc.date.issued1976-
dc.identifier.citationAfr J med med Sci (1976)5, 263-268en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/3065-
dc.descriptionARTICLEen_US
dc.description.abstractThe case history of a typical case of hypokalaemic periodic paralysis is described. A 21-year-old male Uganda n African presented with his second attack of complete flaccid tetraplegia. Serum potassium levels, EGG change s a n d response to therapy were entirely consistent with the diagnosis. Family history was negative. It is possible that this rare disorder has not previously been reported in an African. Possible mechanisms involved in the disorder are briefly discusseden_US
dc.description.sponsorshipCOLLEGE OF MEDICINE,UNIVERSITY OF IBADANen_US
dc.language.isoenen_US
dc.publisherCOLLEGE OF MEDICINEen_US
dc.subjecthypokalaemicen_US
dc.subjecttetraplegiaen_US
dc.subjectserumen_US
dc.subjecttherapyen_US
dc.titleHypokalaemic periodic paralysis in an African—Case reporten_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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