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
Artículo
en Inglés
| 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.
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Índice:
IMSEAR (Asia Sudoriental)
Idioma:
Inglés
Revista:
Indian J Pathol Microbiol
Año:
2016
Tipo del documento:
Artículo
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