ArticleCureus2024
Sjogren's Syndrome Presenting as Hypokalemic Paralysis Secondary to Distal Renal Tubular Acidosis: A Case Report.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Sjögren's Disease-Associated Renal Tubular Acidosis: An Integrated Immuno-Tubular Model of Tubular Dysfunction.International journal of medical sciences · 2026Review
- Hypokalemic rhabdomyolysis due to concurrent distal renal tubular acidosis and Fanconi syndrome in a pediatric patient with Sjögren syndrome.CEN case reports · 2025Article
- Hypokalemic Quadriparesis as the Initial Presentation of Primary Sjögren's Syndrome With Distal Renal Tubular Acidosis: A Case Report.Clinical case reports · 2025Article
- Article
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sjogren's syndrome (SS) is an autoimmune disease affecting multiple exocrine glands such as salivary and lacrimal glands, with focal lymphocytic infiltration. The disease predominantly affects women. The classic presentation is xerostomia and keratoconjunctivitis. In adult populations, tubulointerstitial nephritis, which can manifest as renal tubular acidosis (RTA), is the most prevalent renal manifestation of SS. However, in pediatric populations, RTA only occurs in 7.1-19.2% of cases with renal potassium wasting or hypokalemic paralysis. Here, we describe a case of SS manifesting with hypokalemic paralysis with underlying distal renal tubular acidosis (dRTA).
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