Severe liver dysfunction in an infant with cystic fibrosis masquerading as metabolic liver disease.
Indian J Pathol Microbiol
;
2016 July-Sept 59(3): 339-347
Article
Dans Anglais
| IMSEAR
| ID: sea-179570
ABSTRACT
We present a rare presentation of cystic fibrosis with neonatal cholestasis. Histological features of mucoviscidosis were present in liver involving the biliary tract, intestinal mucosa, pancreas, and lung. Besides, there was a rare association with autosomal dominant type of polycystic renal disease.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
langue:
Anglais
Texte intégral:
Indian J Pathol Microbiol
Année:
2016
Type:
Article
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