Evidence map›Paper›PMID 32830475›Full record

ArticleJournal of clinical research in pediatric endocrinology2021

A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome

Mina Mısırlıgil, Yılmaz Yıldız, Onur Akın, Sevinç Odabaşı Güneş, Mutluay Arslan, Bülent Ünay

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Syndromic forms of congenital hyperinsulinism.Frontiers in endocrinology · 2023
    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

6 authors at 2 institutions in 1 country.

Mina MısırlıgilUniversity of Health Sciences Turkey, Gülhane Faculty of Medicine, Department of Pediatrics, Ankara, TurkeyORCID 0000-0002-7922-5514
Yılmaz YıldızUniversity of Health Sciences Turkey, Gülhane Faculty of Medicine; Dr. Sami Ulus Training and Research Hospital, Clinic of Pediatric Metabolic Diseases, Ankara, TurkeyORCID 0000-0001-9076-1388
Onur AkınUniversity of Health Sciences Turkey, Gülhane Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TurkeyORCID 0000-0002-8430-5519
Sevinç Odabaşı GüneşUniversity of Health Sciences Turkey, Gülhane Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TurkeyORCID 0000-0001-5979-9206
Mutluay ArslanUniversity of Health Sciences Turkey, Gülhane Faculty of Medicine, Department of Pediatric Neurology, Ankara, TurkeyORCID 0000-0002-6520-1810
Bülent ÜnayUniversity of Health Sciences Turkey, Gülhane Faculty of Medicine, Department of Pediatric Neurology, Ankara, TurkeyORCID 0000-0001-5432-8624
Sağlık Bilimleri Üniversitesi · TRMinistry of Health · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kabuki syndrome (KS) is a disease characterized by distinctive facial features, skeletal anomalies and delay in neuromotor development. KS 1 is an autosomal dominant condition caused by mutations in the

Indexed as

Abnormalities, MultipleCongenital HyperinsulinismDNA-Binding ProteinsFaceFemaleHematologic DiseasesHumansInfantNeoplasm ProteinsVestibular DiseasesDNA-Binding ProteinsKMT2D protein, humanNeoplasm ProteinsDiazoxidehyperinsulinemic hypoglycemiaKabuki syndromeKDM6AKMT2

Identifiers

PMID32830475
PMCPMC8638635
OpenAlexW3080429312

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.