A Case of Bartter Syndrome with Muscle Weakness and Short Stature
Journal of the Korean Society of Pediatric Nephrology
;
: 259-265, 2002.
Artigo
em Coreano
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Piúria
/
Síndrome de Bartter
/
Biópsia
/
Debilidade Muscular
/
Alcalose
/
Hematúria
/
Hiperplasia
/
Sistema Justaglomerular
/
Nefrocalcinose
Limite:
Criança
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Society of Pediatric Nephrology
Ano de publicação:
2002
Tipo de documento:
Artigo
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