A Case of Congenital Hemolytic Anemia of Unknown Cause Combined with Gilbert's Syndrome
Korean Journal of Hematology
;
: 58-61, 2008.
Artículo
en Coreano
| WPRIM
| ID: wpr-720811
ABSTRACT
Congenital hemolytic anemia is mainly developed due to intrinsic defects of erythrocytes, but in some cases the cause of hemolytic anemia is unclear. Gilbert's syndrome shows mild, chronic unconjugated hyperbilirubinemia that is due to reduced UDP glucuronosyltransferase (UGT-1A1) activity and this develops because of UGT-1A1 gene mutation. We report here on a case of severe hyperbilirubinemia in a 17-year-old male who was diagnosed with congenital hemolytic anemia of an unknown cause combined with Gilbert's syndrome.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Glucuronosiltransferasa
/
Eritrocitos
/
Enfermedad de Gilbert
/
Hiperbilirrubinemia
/
Anemia Hemolítica
/
Anemia Hemolítica Congénita
Límite:
Adolescente
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Korean Journal of Hematology
Año:
2008
Tipo del documento:
Artículo
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