A Case of Rotor Syndrome / 영남의대학술지
Yeungnam University Journal of Medicine
;
: 257-263, 1989.
Article
Dans Coréen
| WPRIM
| ID: wpr-28067
ABSTRACT
Rotor syndrome is a rare disease of hereditary hyperbilirubinemia transmitted with autosomal recessive trait. In general, Rotor syndrome shows direct hyperbilirubinemia and there has been several reports since Sons's report in 1966, in Korea. A 34-year-old female was admitted with the chief complaint of intermittent icteric sclera for 24 years. There was no family history of jaundice. Rotor syndrome was diagnosed by oral cholecystogram, BSP retention test, 99mTc-DISIDA scan, liver biopsy and electron microscopy study of liver biopsy specimen. We report this case with brief review of the literature.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Sclère
/
Biopsie
/
Microscopie électronique
/
Disofénine de technétium (99mTc)
/
Maladies rares
/
Hyperbilirubinémie héréditaire
/
Hyperbilirubinémie
/
Ictère
/
Corée
/
Foie
Limites du sujet:
Adulte
/
Femelle
/
Humains
Pays comme sujet:
Asie
langue:
Coréen
Texte intégral:
Yeungnam University Journal of Medicine
Année:
1989
Type:
Article
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