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Article

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine - 18 Sept 2026

Zhang Benping, Liu Shengxuan, Zou Biao, Shu Sainan, Dong Chen

Abstract excerpt

Progressive familial intrahepatic cholestasis type 2 (PFIC2) is an autosomal recessive disease caused by homozygous or compound heterozygous mutations in the bile salt export pump (BSEP). The diagnosis has mainly depended on genetic tests. Little research has been conducted to assess the BSEP function, which may help the clinical diagnosis. The present study aimed to quantitatively assess the BSEP function by...

Read the complete abstract on PubMed

Topics

Humans
Cholestasis, Intrahepatic
ATP Binding Cassette Transporter, Subfamily B, Member 11
Female
Bile Acids and Salts
Infant

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Retrospective Studies

Duodenum

Male

Mutation

Child, Preschool

Infant, Newborn

Source

Open in PubMed Open full text

Identifiers

PMID: 42760696
DOI: 10.1097/MD.0000000000050696
PMCID: PMC13593270

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

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