Acute paralysis in the context of hypokalaemia is the presenting feature of a rare group of heterogeneous disorders including the familial periodic paralyses and renal tubular acidosis. Hypokalaemic paralysis has previously been described as the presenting feature of Sjögren's Syndrome. In this report we present a patient with hypokalaemic paralysis, distal renal tubular acidosis and features suggestive of Sjögren's Syndrome.
ChanJC, AlonU.Tubular disorders of acid-base and phosphate metabolism. Nephron.1985; 40: 279.
2.
DeFrancoPE, HaragsimL, SchmitzPG, BastaniB.Absence of vacuolar H(+)-ATPase pump in t collecting duct of a patient with hypokalemic distal renal tubular acidosis and Sjogren's syndromeSoc Nephrol.1995; 6: 295–301.
3.
KaretFE, FinbergKE, NelsonRDMutations in the gene encoding B1 subunit of H+-ATPas cause renal tubular acidosis with sensorineural deafness. Nat Genet.1999; 21: 84–90.