A New Mutation Causing Progressive Familiar Intrahepatic Cholestasis Type 3 in Association with Autoimmune Hepatitis
Background: Some patients exhibit features of both autoimmune hepatitis (AIH) and primary sclerosing cholangitis (PSC). Similarly, patients with progressive familial intrahepatic cholestasis type 3 (PFIC3) may share histological features with PSC. Case report: We report the case of a 22-year-old ma...
Main Authors: | Hugo M Oliveira, Claudia Pereira, Ermelinda Santos-Silva, Jorge Pinto-Basto, José R Vizcaíno, Helena Pessegueiro-Miranda |
---|---|
Format: | Article |
Language: | English |
Published: |
SMC MEDIA SRL
2017-03-01
|
Series: | European Journal of Case Reports in Internal Medicine |
Subjects: | |
Online Access: | http://ejcrim.com/index.php/EJCRIM/article/view/537 |
Similar Items
-
A Rare BSEP Mutation Associated with a Mild Form of Progressive Familial Intrahepatic Cholestasis Type 2
by: Orith Waisbourd-Zinman, et al.
Published: (2017-05-01) -
The role of genetic mutations in intrahepatic cholestasis of pregnancy
by: Gültekin Adanaş Aydın, et al.
Published: (2020-09-01) -
Association of ABCB4 and ABCB11 nucleotide variants with intrahepatic cholestasis of pregnancy
by: Milena Gruszczyńska-Losy, et al.
Published: (2019-12-01) -
BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS (BRIC)
by: S. Arulprakash, et al.
Published: (2010-03-01) -
Case report: progressive familial intrahepatic cholestasis type 3 with compound heterozygous ABCB4 variants diagnosed 15 years after liver transplantation
by: Mariam Goubran, et al.
Published: (2020-11-01)