Medullary sponge kidney presenting with hypokalaemic paralysis

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dc.contributor.authorJayasinghe, K.S.
dc.contributor.authorMendis, B.L.
dc.contributor.authorMohideen, R.
dc.contributor.authorEkanayake, R.A.I.
dc.contributor.authorSheriff, M.H.R.
dc.contributor.authorDharmadasa, K.
dc.date.accessioned2012-02-21T08:56:45Z
dc.date.available2012-02-21T08:56:45Z
dc.date.issued1984
dc.description.abstract:Medullary sponge kidney associated with a defect in urine acidification is rare and usually of no clinical significance. We report a case presenting as hypokalaemic paralysis due to associated congenital distal renal tubular acidosis.
dc.identifier.citationPostgraduate Medical Journal 1984 Apr;60(702):303-4 Vol: 60 No.(702) 1984_.303-4ppen_US
dc.identifier.urihttp://archive.cmb.ac.lk:8080/xmlui/handle/70130/1923
dc.language.isoenen_US
dc.titleMedullary sponge kidney presenting with hypokalaemic paralysisen_US
dc.typeResearch abstracten_US

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