Evidence map›Paper›PMID 38084036›Full record

ReviewJournal of clinical research in pediatric endocrinology2025

Early-onset Chronic Keratitis as the First Presenting Component of Autoimmune Polyendocrine Syndrome Type 1: A Case Report and Review of the Literature

Enver Şimşek, Tülay Şimşek, Oğuz Çilingir

Open access · goldAbstract readCase ReportsReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Journal of clinical research in pediatric endocrinology, 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
0.2field-weighted citation impact, top 38% of its field
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 citations in OpenAlex.

  1. Intracranial infections ofFrontiers in immunology · 2025
    Review
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

3 authors at 1 institution in 1 country.

Enver ŞimşekEskişehir Osmangazi University Faculty of Medicine, Department of Pediatrics, Clinic of Pediatric Endocrinology, Eskişehir, TürkiyeORCID 0000-0003-0120-9976
Tülay ŞimşekEskişehir Osmangazi University Faculty of Medicine, Department of Ophthalmology, Eskişehir, TürkiyeORCID 0000-0001-5132-9066
Oğuz ÇilingirEskişehir Osmangazi University Faculty of Medicine, Department of Medical Genetics, Eskişehir, TürkiyeORCID 0000-0002-5593-4164
Eskişehir Osmangazi University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune polyendocrine syndrome type 1 (APS-1), also referred to as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy, is a rare monogenic autosomal recessive autoimmune disease. It is caused by mutations in the autoimmune regulator (

Indexed as

KeratitisPolyendocrinopathies, AutoimmuneAIRE ProteinChild, PreschoolChronic DiseaseFemaleHumansHypoparathyroidismTranscription FactorsAIRE ProteinTranscription FactorsAIRE mutationAPS1childrenhypoparathyroidismkeratopathy

Identifiers

PMID38084036
PMCPMC12372638
OpenAlexW4389623126

What OpenQuestion 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 OpenQuestion graph.