Results 1 to 10 of about 27,709 (227)
Congenital thrombophilia associated with intrahepatic cholestasis of pregnancy. A case report [PDF]
Folia Medica, 2022 Intrahepatic cholestasis of pregnancy is pregnancy-specific liver disorder, characterized by pruritus as the main clinical symptom, and fasting liver function tests.
Corina Iliadi-Tulbure +4 more
doaj +3 more sources
BMC Pregnancy and Childbirth, 2022 Background Intrahepatic cholestasis of pregnancy is a pregnancy-specific liver disease. In this study, we sought to explore the distribution of lipopolysaccharide in the maternal body, and its effect on the fetal body in the intrahepatic cholestasis of ...
Xiaomei Huang +3 more
doaj +1 more source
The Turkish Journal of Pediatrics, 2023 Background. Benign recurrent intrahepatic cholestasis (BRIC) is a rare cause of cholestasis with recurrent episodes of jaundice and pruritus without extrahepatic bile duct obstruction.
Burcu Berberoğlu Ateş +5 more
doaj +1 more source
Annals of Hepatology, 2021 Introduction and objectives: Differentiating biliary atresia from other causes of neonatal cholestasis is challenging, particularly when cytomegalovirus (CMV) and biliary atresia occur simultaneously.
Dongying Zhao +6 more
doaj +1 more source
Frontiers in Pharmacology, 2022 Cholestasis is caused by intrahepatic retention of excessive toxic bile acids and ultimately results in hepatic failure. Da-Chai-Hu-Tang (DCHT) has been used in China to treat liver and gallbladder diseases for over 1800 years. Here, we demonstrated that
Shihao Xu +16 more
doaj +1 more source
Intrahepatic cholestasis of pregnancy [PDF]
World Journal of Gastroenterology, 2009 Intrahepatic cholestasis of pregnancy is the most common pregnancy-specific liver disease that typically presents in the third trimester. The clinical features are maternal pruritus in the absence of a rash and deranged liver function tests, including raised serum bile acids. Intrahepatic cholestasis of pregnancy is associated with an increased risk of
Williamson, Catherine, Geenes, Victoria
openaire +4 more sources
Compound Heterozygous MYO5B Mutation, a Cause of Infantile Cholestasis: A Case Report
Journal of Nepal Medical Association, 2022 Infantile cholestasis is a common clinical problem in early infancy characterised by impairment in bile formation and/or flow. It requires prompt evaluation for underlying aetiology to initiate appropriate management.
Muna Khanal +2 more
doaj +1 more source
Dengue fever as a potential cause of sickle cell intrahepatic cholestasis: A report of two cases
Revista da Sociedade Brasileira de Medicina Tropical, 2021 Sickle cell intrahepatic cholestasis is a potentially fatal syndrome characterized by jaundice, painful hepatomegaly, and organ dysfunction. Two cases of sickle cell intrahepatic cholestasis associated with dengue fever were described. Endothelial damage/
Leonardo Rodrigues de Oliveira +5 more
doaj +1 more source
A Complex Case of Cholestasis in a Patient with ABCB4 and ABCB11 Mutations [PDF]
, 2018 The low-phospholipid-associated cholelithiasis (LPAC) syndrome is a form of symptomatic cholelithiasis occurring in young adults, characterized by recurrence of symptoms after cholecystectomy and presence of hepatolithiasis.
Anapaz, V +7 more
core +1 more source
Benign Recurrent Intrahepatic Cholestasis in Pregnancy: Fetal Death at 36 Weeks of Gestation
Case Reports in Obstetrics and Gynecology, 2021 Introduction. Benign recurrent intrahepatic cholestasis is a rare hepatologic disorder characterized by recurrent, self-limited episodes of severe pruritus, jaundice, and elevated bile acids.
Mariam Ayyash +4 more
doaj +1 more source