Sjogren's Syndrome Manifested as Hypokalemic Paralysis
Ting-Ting See, Siu-Pak Lee, Hua-Fen Chen, Ju‐Ying Jiang, Chih‐Yuan Wang, Hsinyu Lee
Abstract
Ting-Ting See, Siu-Pak Lee, Hua-Fen Chen, Ju‐Ying Jiang, Chih‐Yuan Wang, Hsinyu Lee
Abstract
A 31-year old woman was admitted for hypokalemic paralysis. Laboratory examination revealed hyperchloremic metabolic acidosis with a positive urinary anion gap compatible with distal renal tubular acidosis (DRTA). Her sicca symptom, as well as positive autoimmune studies pointed to the underlying cause as a case of Sjogren's syndrome. The complications of DRTA include life threatening hypokalemia, nephrolithiasis, chronic renal failure, growth retardation and osteomalacia. These co-morbidities can be avoided if the diagnosis is made early and life long potassium alkali salt replacement is maintained.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
A 31-year old woman was admitted for hypokalemic paralysis. Laboratory examination revealed hyperchloremic metabolic acidosis with a positive urinary anion gap compatible with distal renal tubular acidosis (DRTA). Her sicca symptom, as well as positive autoimmune studies pointed to the underlying cause as a case of Sjogren's syndrome. The complications of DRTA include life threatening hypokalemia, nephrolithiasis, chronic renal failure, growth retardation and osteomalacia. These co-morbidities can be avoided if the diagnosis is made early and life long potassium alkali salt replacement is maintained.
Key concepts: Distal renal tubular acidosis, Hypokalemia, Medicine, Renal tubular acidosis, Osteomalacia, Metabolic acidosis, Paralysis, Hypokalemic periodic paralysis