Evidence map›Paper›PMID 34589361›Full record

ArticleCureus2021

Liver Abscesses as a Sign of Chronic Granulomatous Disease in Adolescent.

Hussain A Al Ghadeer, Fadi N Busaleh, Jaber A Al Habeeb, Rabab M Alaithan, Abdullah E Almutahhar, Murtadha M Bin Abd, Mishael M Aldawood

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

Article in Cureus, 2021. 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 49% 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, 3 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Hussain A Al GhadeerPediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Fadi N BusalehPediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Jaber A Al HabeebAllergy and Immunology, Maternity and Children Hospital, AlAhsa, SAU.
Rabab M AlaithanPediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Abdullah E AlmutahharPediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Murtadha M Bin AbdPediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Mishael M AldawoodPediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Maternity and Children's Hospital · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic granulomatous disease (CGD) is an inherited primary immunodeficiency disease caused by a genetic defect in the nicotinamide adenine dinucleotide phosphate oxidase (NADPH) complex that affects phagocytes. This leads to recurrent severe bacterial and fungal infections manifested by recurrent pneumonia, also involving soft tissue, bones, and liver. Usually, CGD is presented and diagnosed in the first five years of life. In this case report, we describe a late presentation in an adolescent with multiple liver abscesses, the approach of diagnosis, and management.

Indexed as

chronic granulomatous diseaseliver abscessnadph oxidase deficiencyprimary immunodeficiency disorderx-linked genetic diseases

Identifiers

PMID34589361
PMCPMC8464347
OpenAlexW3193628593

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.