A Case of Bartter Syndrome with Muscle Weakness and Short Stature
Journal of the Korean Society of Pediatric Nephrology
;
: 259-265, 2002.
Article
Dans Coréen
| WPRIM
| ID: wpr-216051
ABSTRACT
Bartter syndrome is a rare disorder characterized by the association of hypokalemic hypochloremic metabolic alkalosis, hyperreninemia, hyperaldosteronemia, short stature and nephrocalcinosis. This disorder presents with hyperplasia of juxtaglomerular apparatus on renal biopsy. We experienced a case of late-onset Bartter syndrome with nephrocalcinosis in a 9-year-old boy, whose chief pictures were muscle weakness, short stature, persistent sterile pyuria and microscopic hematuria. We report this case with a brief review of related literatures.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Pyurie
/
Syndrome de Bartter
/
Biopsie
/
Faiblesse musculaire
/
Alcalose
/
Hématurie
/
Hyperplasie
/
Appareil juxtaglomérulaire
/
Néphrocalcinose
Limites du sujet:
Enfant
/
Humains
/
Mâle
langue:
Coréen
Texte intégral:
Journal of the Korean Society of Pediatric Nephrology
Année:
2002
Type:
Article
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