Results 131 to 140 of about 3,364 (172)

Dubin-Johnson and Rotor Syndromes: A Review and Update of Pathophysiological Mechanisms. [PDF]

J Clin Transl Hepatol
Thakkar B, Wu GY.
europepmc   +1 more source

Familial cholestasis: Progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy

Bailliere's Best Practice and Research in Clinical Gastroenterology, 2010
Progressive familial intrahepatic cholestasis (PFIC) type 1, 2 and 3 are due to mutations in ATP8B1, ABCB11 and ABCB4, respectively. Each of these genes encodes a hepatocanalicular transporter, which is essential for the proper formation of bile. Mutations in ABCB4 can result in progressive cholestatic disease, while mutations in ATP8B1 and ABCB11 can ...
Saskia W C Van Mil, Janneke M Stapelbroek, Leo W J Klomp   +2 more
exaly   +5 more sources

Benign recurrent intrahepatic cholestasis

The Indian Journal of Pediatrics, 2005
Benign recurrent intrahepatic cholestasis (BRIC) is a rare cause of cholestasis in children. The disease may start in infancy or early childhood. Jaundice persists or recurs throughout life but does not lead to chronic liver disease or cirrhosis. Treatment is mostly symptomatic. The condition has not been reported in Indian children.
V, Gupta, M, Kumar, Baldev D, Bhatia
openaire   +3 more sources

Benign Recurrent Intrahepatic Cholestasis

Journal of Clinical Gastroenterology, 1989
Benign recurrent intrahepatic cholestasis is characterized by attacks of cholestasis. The purpose of our study of 26 patients was to emphasize some features uncommonly or never reported in this disease: (a) in each patient, the attacks of cholestasis were stereotypic; (b) attacks of cholestasis were not associated with pruritus in 15% of our patients; (
R, Brenard, A P, Geubel, J P, Benhamou
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Benign Recurrent Intrahepatic Cholestasis

New England Journal of Medicine, 1963
INTRAHEPATIC cholestasis as a manifestation of liver disease is not an unusual finding. Such obstruction to bile flow may occur quite frequently in acute and chronic hepatitis and primary biliary c...
Robert H Schapiro, Kurt J Isselbacher, Schapiro Robert H   +2 more
exaly   +5 more sources

Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis

American Journal of Medical Genetics Part A, 1995
AbstractBenign recurrent intrahepatic cholestasis BRIO is a rare disorder characterized by recurrent episodes of cholestasis without permanent liver damage. Familial and sporadic cases have been described. Based on existing evidence, both autosomal‐recessive and autosomal‐dominant inheritance have been considered.
Tom J de Koning, Lodewijk A Sandkuijl, Frits A Beemer   +2 more
exaly   +3 more sources

Benign recurrent intrahepatic cholestasis. A clinico-pathologic study

Research in Clinic and Laboratory, 1990
Authors report 6 cases of benign recurrent intrahepatic cholestasis (BRIC), a rare disease of unknown etiology first described 30 years ago by Summerskill and Walshe, and thought to represent a study model for human cholestasis. Clinical, biochemical and pathologic findings of BRIC are briefly summarized in this paper in order to emphasize some ...
Mario Rizzetto, Giorgio Verme, Rizzetto Mario   +2 more
exaly   +3 more sources

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

Gastroenterology, 2004
Background & Aims: Progressive familial intrahepatic cholestasis (PFIC) and benign recurrent intrahepatic cholestasis (BRIC) are hereditary liver disorders; PFIC is characterized by severe progressive liver disease whereas BRIC patients have intermittent
Saskia W C Van Mil, Ekkehard Sturm, Laura N Bull   +2 more
exaly   +3 more sources