A rare cause of carpal tunnel syndrome in childhood: Benign recurrent intrahepatic cholestasis
Open Medicine, 2010 Carpal tunnel syndrome and benign recurrent intrahepatic cholestasis are rare conditions in childhood. Benign intrahepatic cholestasis is characterized by repeated self-limited attacks of cholestasis that can start at any age and last from weeks to ...
Balamtekin Necati +4 more
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Description of Two New ABCB11 Mutations Responsible for Type 2 Benign Recurrent Intrahepatic Cholestasis in a French-Canadian Family [PDF]
Canadian Journal of Gastroenterology, 2011 Benign recurrent intrahepatic cholestasis is a rare clinical entity that is caused by mutations in the canalicular transport genes. The present report describes two individuals from the same family whose symptoms were typical of the clinical ...
Yannick Beauséjour +3 more
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A 19-year-old Patient with Recurrent Pruritus and Jaundice
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2023 Аim: to highlight the importance of broad differential diagnosis and possibility of conversion of benign recurrent intrahepatic cholestasis type 2 into more aggressive clinical phenotype.Key points. A 19-year-old female patient was admitted to the Clinic
K. S. Nezhdanov +5 more
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Sepsis as a cause of intrahepatic cholestasis [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2009 Introduction. The causes of intrahepatic cholestasis include cholestatic viral hepatitis, primary biliary cirrhosis, benign recurrent cholestasis, primary sclerosing cholangitis and sepsis.
Rudić Jelena +5 more
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"An Iranian girl with benign recurrent intrahepatic cholestasis " [PDF]
Acta Medica Iranica, 2002 This report presents an 11 year-old girl with benign recurrent cholestasis (BRIC) who developed episodes of severe jaundice and pruritus at the ages of 2.5 and 10 years. Each episode lasted for 3-4 months.
Kavehmanesh Z +1 more
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New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical Implications
Canadian Journal of Gastroenterology and Hepatology, 2018 Cholestasis is characterised by impaired bile secretion and accumulation of bile salts in the organism. Hereditary cholestasis is a heterogeneous group of rare autosomal recessive liver disorders, which are characterised by intrahepatic cholestasis ...
Eva Sticova +2 more
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Case Report: A Rare Heterozygous ATP8B1 Mutation in a BRIC1 Patient: Haploinsufficiency?
Frontiers in Medicine, 2022 Benign recurrent intrahepatic cholestasis (BRIC) is an autosomal recessive disorder characterized by recurrent cholestasis. ATPase class I, type 8B, member 1 (ATP8B1) encodes familial intrahepatic cholestasis 1 (FIC1), which acts as a phosphatidylserine ...
Hao Bing +5 more
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Indian Journal of Pathology and Microbiology, 2021 ABCB11 deficiency, formerly benign recurrent intrahepatic cholestasis (BRIC) is a very rare hereditary disorder characterized by the recurrent and intermittent episodes of cholestasis, jaundice, and pruritus.
K V Kalaranjini +3 more
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Erratum to “A sporadic case of benign recurrent intrahepatic cholestasis in a growth-impaired young male” [PDF]
Science Progressdoaj +2 more sources
Maternal and Foetal Outcomes in Early and Late Intrahepatic Cholestasis of Pregnancy and their Association with Maternal Serum Bile Acid Levels: A Prospective Cohort Study [PDF]
Journal of Clinical and Diagnostic Research, 2022 Introduction: Intrahepatic Cholestasis of Pregnancy (IHCP) also known as recurrent jaundice of pregnancy is a pregnancy specific benign liver disease presenting in the second and third trimester of pregnancy and is associated with increased perinatal ...
Sangeeta Gupta +3 more
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