Plasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infant.
Southeast Asian J Trop Med Public Health
;
1999 ; 30 Suppl 2(): 140-2
Artículo
en Inglés
| IMSEAR
| ID: sea-30766
ABSTRACT
Methylmalonic acidemia is an inborn error of organic acid metabolism resulting from defects in methylmalonyl CoA mutase. Analysis of plasma free amino acids in a 15-month-old Thai infant by HPLC showed marked elevation of glycine. HPLC analysis of urinary organic acids showed high levels of methylmalonic acid.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Femenino
/
Humanos
/
Ácidos Carboxílicos
/
Errores Innatos del Metabolismo de los Aminoácidos
/
Aminoácidos
/
Lactante
/
Ácido Metilmalónico
Idioma:
Inglés
Revista:
Southeast Asian J Trop Med Public Health
Año:
1999
Tipo del documento:
Artículo
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