A Case of Citrullinemia Controlled by Diet and Arginine
Journal of the Korean Society of Neonatology
; : 280-280, 1999.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-73916
Biblioteca responsável:
WPRO
ABSTRACT
Citrullinemia is an inborn error of urea cycle metabolism caused by deficiency of arginosuccinate synthetase. It is characterized by hyperammonemia and high citrulline level in serum, CSF and urine. The clinical symptoms include vomiting, lethargy, seizure, coma and ultimately death if hyperammonemia is not controlled. We report a case of 9- day old male with citrullinemia who was initially treated with sodium benzoate during acute stage followed by gradual weaning to discontinuation. Hyperammonemia was well controlled by low protein milk diet and arginine.
Texto completo:
Disponível
Contexto em Saúde:
ODS3 - Meta 3.4 Reduzir as mortes prematuras devido doenças não transmissíveis
Problema de saúde:
Doenças do Sistema Endócrino
/
Epilepsia
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Arginina
/
Convulsões
/
Ureia
/
Vômito
/
Desmame
/
Citrulina
/
Coma
/
Benzoato de Sódio
/
Citrulinemia
/
Hiperamonemia
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Society of Neonatology
Ano de publicação:
1999
Tipo de documento:
Artigo