Benign Recurrent Intrahepatic Cholestasis with a Single Heterozygote Mutation in the ATP8B1 Gene
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ÀÌÀ±¼® ( Lee Yun-Seok )
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼¿ïº´¿ø ¼Ò¾Æû¼Ò³â°ú
±è¹ÌÁø ( Kim Mi-Jin )
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±ââ¼® ( Ki Chang-Seok )
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ÀÌÀ¯¹Î ( Lee Yoo-Min )
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼¿ïº´¿ø ¼Ò¾Æû¼Ò³â°ú
ÀÌÀ± ( Lee Yoon )
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼¿ïº´¿ø ¼Ò¾Æû¼Ò³â°ú
ÃÖ¿¬È£ ( Choe Yon-Ho )
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KMID : 0816120120150020122
Abstract
Benign recurrent intrahepatic cholestasis (BRIC) is a rare autosomal recessive inherited disorder characterized by multiple recurrent episodes of severe cholestatic jaundice without obstruction of extrahepatic bile duct. We present the case of a 7-year-old boy with BRIC confirmed by mutation analysis in the ATP8B1 gene and typical clinical manifestation. Despite inheritance of BRIC, we detected a mutation on only one allele. To our knowledge, this is the first report of BRIC with a confirmed single heterozygote novel mutation in the ATP8B1 gene in Korea.
Å°¿öµå
Intrahepatic cholestasis; Single heterozygote; ATP8B1 gene
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