A Case of Gitelman Syndrome
Soonchunhyang Medical Science
; : 145-147, 2012.
Article
em Ko
| WPRIM
| ID: wpr-110155
Biblioteca responsável:
WPRO
ABSTRACT
Gitelman's syndrome is an autosomal recessive disorder characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria that has recently been reported to be linked to thiazide-sensitive Na-Cl cotransporter gene mutation. We have experienced one patient whose initial complaint was paresthesia of hand and feet, who had hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. We report the case of Gitelman's syndrome with a brief review of related literature.
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Base de dados:
WPRIM
Limite:
Humans
Idioma:
Ko
Ano de publicação:
2012
Tipo de documento:
Article