Evidence map›Paper›PMID 42183258›Full record

ArticleFrontiers in immunology2026

Case Report: Severe neonatal lupus in an infant with homozygous

Xiaojing Yu, Jiwu Lou, Yuli Zhong, Lan Zhang

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 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

4 authors.

Xiaojing YuDepartment of Pediatrics, Zhongshan City People's Hospital, Zhongshan, China.
Jiwu LouPrenatal Diagnosis Center, Dongguan Maternal and Child Health Care Hospital, Dongguan, China.
Yuli ZhongDepartment of Neonatology, Dongguan Maternal and Child Health Care Hospital, Dongguan, China.
Lan ZhangDepartment of Neonatology, Dongguan Maternal and Child Health Care Hospital, Dongguan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neonatal lupus erythematosus (NLE) is a rare, passively acquired autoimmune disease. The manifestations of NLE are varied, and the outcomes of the majority of cases result in spontaneous resolution. However, severe cases are limited. Emerging evidence highlights the genetic heterogeneity of NLE. The missense variant p.Arg90His in

Indexed as

Chromosomes, Human, Pair 14Chromosomes, Human, Pair 4Lupus Erythematosus, SystemicMutation, MissenseNADPH OxidasesTranslocation, GeneticFemaleHomozygoteHumansInfant, NewbornNADPH Oxidasesneutrophil cytosolic factor 1der(14)t(4;14) translocationgenetic lesionhomozygous variantNCF1neonatal lupus erythematosus

Identifiers

PMID42183258
PMCPMC13194358

What OpenQuestion holds

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Registered trials

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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.