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PFIC type III in infant presenting as acute liver cell failure
Syed Ahmed Zaki1, Preeti Shanbag, Anjali Amarapurkar
1Department of Pediatrics, Lokmanya Tilak Municipal Medical College and General Hospital, Mumbai-400 022, India.
Indian Journal of Pathology & Microbiology
|June 17, 2010
Summary
A rare infant liver disease, Byler disease or progressive familial intrahepatic cholestasis type III, can cause acute liver failure. Early diagnosis is crucial for managing this severe condition in infants.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Medical Genetics
Background:
- Progressive familial intrahepatic cholestasis (PFIC) encompasses genetic disorders affecting bile transport.
- Byler disease, a form of PFIC III, presents in infancy with severe cholestasis and rapid progression.
- Consanguinity in parents increases the risk of autosomal recessive genetic liver diseases.
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