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CLINICO-PATHOLOGY CONFERENCE
Year : 2016  |  Volume : 59  |  Issue : 3  |  Page : 339-347

Severe liver dysfunction in an infant with cystic fibrosis masquerading as metabolic liver disease


1 Department of Pediatric Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
2 Advanced Pediatric Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India
3 Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India

Correspondence Address:
Prof. Kim Vaiphei
Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh - 160 012
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0377-4929.188137

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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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