Answers are grounded in this paper and cite their sources.
Case report demonstrates liver disease due to KIF12 mutation in a child, suggesting importance of molecular diagnostics.
This case report describes a 7-year-old boy with progressive familial intrahepatic cholestasis (PFIC) type 8 caused by a homozygous KIF12 mutation, presenting with jaundice, severe pruritus, digital clubbing, and advanced liver disease. The diagnosis was confirmed through a comprehensive evaluation integrating clinical findings, biochemical profiling, imaging, and whole-exome sequencing. Clinical images of clubbing and icterus enhance the diagnostic narrative, emphasizing key physical signs. This case contributes to the sparse literature on PFIC8, highlighting the critical role of molecular diagnostics in rare liver diseases and advocating for increased awareness and research into this understudied subtype of familial intrahepatic cholestasis.
No takes yet. Share an insight, caveat, or question.
Jayachandra et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: