Evidence map›Paper›PMID 38385051›Full record

ArticleClinical case reports2024

Case report of congenital neutropenia type 4 with glucose-6-phosphatase catalytic subunit 3 (G6PC3) deficiency.

Nabil S Dhayhi, Mohammed A Mahnashi, Alanoud I Mokhasha, Lana F Ahmed, Ahmed E Shamakhi, Adeeb A Ageel, Mohammed A Tohary, Abdulaziz H Alhazmi

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

Article in Clinical case reports, 2024. 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
0.6field-weighted citation impact, top 31% 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, 1 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 2 institutions in 1 country.

Nabil S DhayhiPediatric Infectious Disease Unit King Fahad Central Hospital Jazan Saudi Arabia.
Mohammed A MahnashiPediatric Genetic Diseases Unit King Fahad Central Hospital Jazan Saudi Arabia.
Alanoud I MokhashaPediatric Department King Fahad Central Hospital Jazan Saudi Arabia.
Lana F AhmedPediatric Department King Fahad Central Hospital Jazan Saudi Arabia.
Ahmed E ShamakhiPediatric Allergy/Immunology Unit King Fahad Central Hospital Jazan Saudi Arabia.
Adeeb A AgeelPediatric Hematology Unit Kung Fahad Central Hospital Jazan Saudi Arabia.
Mohammed A ToharyPediatric Hematology Unit Kung Fahad Central Hospital Jazan Saudi Arabia.
Abdulaziz H AlhazmiFaculty of Medicine Jazan University Jazan Saudi Arabia.ORCID https://orcid.org/0000-0002-4260-6540
King Fahad Central Hospital · SAJazan University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital neutropenia syndromes encompass a group of genetic disorders characterized by persistent neutropenia and recurrent infections inherited in an autosomal recessive, dominant, or X-linked manner. These syndromes arise from mutations in various genes, and one of the significant genes involved is glucose-6-phosphatase catalytic subunit 3 (

Indexed as

abscesscongenital neutropeniaDursun syndromeimmune deficiencyJazanSaudi Arabia

Identifiers

PMID38385051
PMCPMC10879636
OpenAlexW4392002172

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.