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Rheumatoid arthritis accompanied by Gitelman syndrome / 영남의대학술지
Article in Ko | WPRIM | ID: wpr-84530
Responsible library: WPRO
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.
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Full text: 1 Index: WPRIM Main subject: Paralysis / Arthritis, Rheumatoid / Tremor / Genetic Testing / Alkalosis / Thiazides / Gitelman Syndrome / Fatigue / Solute Carrier Family 12, Member 3 / Furosemide Limits: Adult / Humans Language: Ko Journal: Yeungnam University Journal of Medicine Year: 2017 Type: Article
Full text: 1 Index: WPRIM Main subject: Paralysis / Arthritis, Rheumatoid / Tremor / Genetic Testing / Alkalosis / Thiazides / Gitelman Syndrome / Fatigue / Solute Carrier Family 12, Member 3 / Furosemide Limits: Adult / Humans Language: Ko Journal: Yeungnam University Journal of Medicine Year: 2017 Type: Article