Caroli's Syndrome with Autosomal Recessive Polycystic Kidney Disease in a Two Month Old Infant
Yonsei Medical Journal
;
: 131-134, 2006.
Article
Dans Anglais
| WPRIM
| ID: wpr-116909
ABSTRACT
Caroli's syndrome is a rare congenital disorder that involves intrahepatic bile duct ectasia and congenital hepatic fibrosis, frequently seen with concomitant autosomal recessive polycystic kidney disease (ARPKD). Literature on infants with ARPKD is rare. Here, we present a case of a two month old boy who was diagnosed with Caroli's syndrome and ARPKD.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Polykystose rénale autosomique récessive
/
Maladie de Caroli
/
Conduit hépatique commun
/
Rein
Limites du sujet:
Humains
/
Bébé
/
Mâle
langue:
Anglais
Texte intégral:
Yonsei Medical Journal
Année:
2006
Type:
Article
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