Renal tubular acidosis, arthritis and autoantibodies: primary Sjögren's syndrome in childhood

Abstract
Sir, Primary Sjögren's syndrome (PSS) is rare in the paediatric population [1, 2]. We describe an 8-yr-old female who presented with arthritis, distal renal tubular acidosis and an autoantibody profile suggestive of Sjögren's syndrome without sicca symptoms.

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