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Medullary sponge kidney presenting with hypokalaemic paralysis.
  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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