A Case of Gitelman Syndrome
Soonchunhyang Medical Science
; : 145-147, 2012.
Article
in Ko
| WPRIM
| ID: wpr-110155
Responsible library:
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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Paresthesia
/
Receptors, Drug
/
Alkalosis
/
Sodium Chloride Symporters
/
Gitelman Syndrome
/
Foot
/
Hand
/
Hypokalemia
Limits:
Humans
Language:
Ko
Journal:
Soonchunhyang Medical Science
Year:
2012
Type:
Article