Evidence map›Paper›PMID 42358581›Full record

ArticleFrontiers in pediatrics2026

Clinical and genetic characteristics of children with sodium taurocholate cotransporting poly-peptide deficiency.

Lina Du, Mengyao Zhou, Jing Yang, Min Du, Maolin Jiang, Lijing Xiong

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lina Du *Department of Pediatric Gastroenterology, Chengdu Women and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology, Chengdu, Sichuan, China.
Mengyao Zhou *Department of Pediatric Gastroenterology, Chengdu Women and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology, Chengdu, Sichuan, China.
Jing YangDepartment of Pediatric Gastroenterology, Chengdu Women and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology, Chengdu, Sichuan, China.
Min DuDepartment of Pediatric Gastroenterology, Chengdu Women and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology, Chengdu, Sichuan, China.
Maolin JiangDepartment of Pediatric Gastroenterology, Chengdu Women and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology, Chengdu, Sichuan, China.
Lijing XiongDepartment of Pediatric Gastroenterology, Chengdu Women and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology, Chengdu, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Sodium taurocholate cotransporting polypeptide deficiency (NTCPD) is an autosomal recessive disorder caused by Methods: We conducted a retrospective review of clinical and genetic data from children diagnosed with NTCPD between September 2020 and August 2024, and performed a 12-month observational follow-up. Results: This study included 19 children who exhibited heterogeneous clinical presentations. The participants were categorized into a jaundice group ( Discussion: This study expands the clinical data of Chinese children with NTCPD, confirming the predominance of the c.800C > T mutation and revealing phenotypic heterogeneity alongside generally favorable outcomes. Elevated

Indexed as

case serieshyperbileacidemiahypercholanemiaNTCPSLC10A1 gene

Identifiers

PMID42358581
PMCPMC13290667

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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 OpenQuestion graph.