Evidence map›Paper›PMID 33975400›Full record

ArticleJournal of Korean medical science2021

Empty Sella Syndrome Associated with Growth Hormone Deficiency: the First Case Report of Weiss-Kruszka Syndrome.

Jisun Park, Dong Jun Ha, Go Hun Seo, Seri Maeng, Sung Mo Kang, Sujin Kim, Ji Eun Lee

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of Korean medical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Novel variants inTranslational pediatrics · 2025
    Article
  4. A Nonsense Variant ofFrontiers in genetics · 2022
    Article
  5. Case report: A heterozygous mutation inFrontiers in genetics · 2022
    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

7 authors at 2 institutions in 1 country.

Jisun ParkDepartment of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0003-3793-6577
Dong Jun HaDepartment of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0002-4331-6801
Go Hun Seo3 Billion Inc., Seoul, Korea.ORCID https://orcid.org/0000-0003-1518-1791
Seri MaengNorthwest Gyeonggi Regional Center for Rare Disease, Inha University Hospital, Incheon, Korea.ORCID https://orcid.org/0000-0001-6850-5548
Sung Mo KangNorthwest Gyeonggi Regional Center for Rare Disease, Inha University Hospital, Incheon, Korea.ORCID https://orcid.org/0000-0001-7722-596X
Sujin KimDepartment of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0003-0893-0512
Ji Eun LeeDepartment of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.ORCID https://orcid.org/0000-0002-7386-0015
Inha University Hospital · KRInha University · KR

Funding

Inha University
6 · The paper itself

Abstract

Weiss-Kruszka syndrome (WSKA), caused by heterozygous loss-of-function variants in

Indexed as

AdolescentDNA-Binding ProteinsEmpty Sella SyndromeGrowth HormoneHumansIntellectual DisabilityMaleNerve Tissue ProteinsTranscription FactorsDNA-Binding ProteinsGrowth HormoneNerve Tissue ProteinsTranscription FactorsZNF462 protein, humanEmpty SellaGrowth Hormone DeficiencyWeiss-Kruszka SyndromeZNF462

Identifiers

PMID33975400
PMCPMC8111047
OpenAlexW3158103871

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.