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Rheumatoid arthritis accompanied by Gitelman syndrome / 영남의대학술지
Article em Ko | WPRIM | ID: wpr-84530
Biblioteca responsável: 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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Texto completo: 1 Índice: WPRIM Assunto principal: Paralisia / Artrite Reumatoide / Tremor / Testes Genéticos / Alcalose / Tiazidas / Síndrome de Gitelman / Fadiga / Membro 3 da Família 12 de Carreador de Soluto / Furosemida Limite: Adult / Humans Idioma: Ko Revista: Yeungnam University Journal of Medicine Ano de publicação: 2017 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Paralisia / Artrite Reumatoide / Tremor / Testes Genéticos / Alcalose / Tiazidas / Síndrome de Gitelman / Fadiga / Membro 3 da Família 12 de Carreador de Soluto / Furosemida Limite: Adult / Humans Idioma: Ko Revista: Yeungnam University Journal of Medicine Ano de publicação: 2017 Tipo de documento: Article