A Case of Gitelman Syndrome
Soonchunhyang Medical Science
; : 145-147, 2012.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| 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.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Parestesia
/
Receptores de Droga
/
Alcalose
/
Simportadores de Cloreto de Sódio
/
Síndrome de Gitelman
/
Pé
/
Mãos
/
Hipopotassemia
Limite:
Humanos
Idioma:
Coreano
Revista:
Soonchunhyang Medical Science
Ano de publicação:
2012
Tipo de documento:
Artigo