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
in English
| 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.
Full text:
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Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian J Pathol Microbiol
Year:
2016
Type:
Article
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