1.
Southeast Asian J Trop Med Public Health
;
1999 ; 30 Suppl 2(): 149-50
Artículo
en Inglés
| IMSEAR
| ID: sea-35872
RESUMEN
We found a 4-year-old boy in the screened cohort, who showed a low ceruloplasmin (CP) in urine (17 ng/mg-creatinine) and in blood (0.6 mg/dl), but his urine copper was in the normal range. Furthermore this child was diagnosed as Wilson disease (WD) by genetic analysis. Although no significant correlation was observed between urine and blood levels of CP, it is conceivable that WD may be accompanied by very low concentration of urine CP.
Asunto(s)
Ceruloplasmina/análisis , Preescolar , Cobre/orina , Degeneración Hepatolenticular/diagnóstico , Humanos , Masculino , Tamizaje Masivo
2.
Asian Pac J Allergy Immunol
;
1984 Jun; 2(1): 77-84
Artículo
en Inglés
| IMSEAR
| ID: sea-36616