Evidence map›Paper›PMID 39814052›Full record

ReviewZeitschrift fur Geburtshilfe und Neonatologie2025

Whole-exome sequencing identifies novel mutation in intrahepatic cholestasis of pregnancy: A case report and literature review.

Xixi Deng, Xueqi Li, Yongchi Zhan, Yuxin Ren, Tingting Xu, Xiaodong Wang

Abstract readCase ReportsReviewCase Reports
In one paragraph

Review in Zeitschrift fur Geburtshilfe und Neonatologie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Molecular mechanism of substrate transport by human peroxisomal ABCD3.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Xixi DengDepartment of Obstetrics and Gynecology, Sichuan University West China Second University Hospital, Chengdu, China.
Xueqi LiDepartment of Obstetrics and Gynecology, Sichuan University West China Second University Hospital, Chengdu, China.
Yongchi ZhanDepartment of Obstetrics and Gynecology, Sichuan University West China Second University Hospital, Chengdu, China.
Yuxin RenDepartment of Obstetrics and Gynecology, Sichuan University West China Second University Hospital, Chengdu, China.
Tingting Xu *Department of Obstetrics and Gynecology, Sichuan University West China Second University Hospital, Chengdu, China.
Xiaodong Wang *Department of Obstetrics and Gynecology, Sichuan University West China Second University Hospital, Chengdu, China.ORCID 0000-0002-0164-1251

Funding

Key Research and Development Project by Department of Science and Technology in Sichuan Province 2022YFS0042National Natural Science Foundation for Young Scientists of China 82001560Science Foundation for Young Scientists of Sichuan Province 2023NSFSC1608
6 · The paper itself

Abstract

Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy-specific liver disease characterized by pruritus and elevated total bile acid (TBA) levels. The most serious impact of ICP is sudden unexplained intrauterine fetal death, especially when an associated TBA ≥ 100 µmol/L is confirmed.We report a case of a 27-year-old female patient with early-onset severe refractory ICP. Whole-exome sequencing and mutation analyses were performed to obtain genetic data on the patient and her mother. Sanger sequencing was performed to screen the mutation site. Computer-based algorithms were applied to predict the pathogenesis of the identified mutation. Subsequently, we conducted a literature review to characterize the pathological features and perinatal management of severe refractory ICP, especially ICP with genetic susceptibility.A heterozygous mutation in the

Indexed as

ATP Binding Cassette Transporter, Subfamily DCholestasis, IntrahepaticExome SequencingMutationPregnancy ComplicationsAdultATP-Binding Cassette TransportersFemaleGenetic Predisposition to DiseaseHumansLive BirthPregnancyPrenatal DiagnosisABCD3 protein, humanATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily D

Identifiers

PMID39814052
PMCPMC12334265

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.