Yeungnam Univ J Med.  2017 Jun;34(1):101-105. 10.12701/yujm.2017.34.1.101.

Rheumatoid arthritis accompanied by Gitelman syndrome

Affiliations
  • 1Division of Rheumatology, Department of Internal Medicine, Maryknoll Medical Center, Busan, Korea. ete@lycos.co.kr

Abstract

Gitelman syndrome is a condition caused by a mutation of the thiazide sensitive Na-Cl cotransporter gene on the distal convoluted tubule. It results in a variety of clinical features, including hypokalemia, hypomagnesemia, hypocalciuria, and metabolic alkalosis. It is often diagnosed in asymptomatic adults presented with unexplained hypokalemia; however, it is sometimes associated with muscular cramps, numbness, fatigue, weakness, or paralysis. We experienced a case of rheumatoid arthritis accompanied by Gitelman syndrome, presented with hand tremor. We diagnosed her using renal clearance study and genetic analysis. Here, we report our experiences regarding this case along with a literature review.

Keyword

Gitelman syndrome; Rheumatoid arthritis; Furosemide; Thiazides; Genetic testing

MeSH Terms

Adult
Alkalosis
Arthritis, Rheumatoid*
Fatigue
Furosemide
Genetic Testing
Gitelman Syndrome*
Hand
Humans
Hypesthesia
Hypokalemia
Muscle Cramp
Paralysis
Solute Carrier Family 12, Member 3
Thiazides
Tremor
Furosemide
Thiazides
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