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Medullary sponge kidney presenting with hypokalaemic paralysis.
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  1. K. S. Jayasinghe,
  2. B. L. Mendis,
  3. R. Mohideen,
  4. R. Ekanayake,
  5. M. H. Sheriff,
  6. K. Dharmadasa

    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.

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