Evidence map›Paper›PMID 41809613›Full record

ArticleSultan Qaboos University medical journal2026

Novel

Azzeddine Laaraje, Khadija Belcadi Abassi, Mouna Lemaamer, Abdelilah Radi, Amale Hassani, Rachid Abilkassem

Abstract readCase Reports
In one paragraph

Article in Sultan Qaboos University medical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Azzeddine LaarajeDepartment of Pediatrics, Mohammed V Military Teaching Hospital, Mohammed V University in Rabat, Rabat, Morocco.ORCID 0000-0002-7393-7473
Khadija Belcadi AbassiDepartment of Pediatrics, Rabat Children's Hospital, Rabat, Morocco.ORCID 0009-0000-0078-5141
Mouna LemaamerLaboratory of Human Pathologies, Mohammed V University in Rabat, Rabat, Morocco.ORCID 0000-0001-6553-3244
Abdelilah RadiDepartment of Pediatrics, Mohammed V Military Teaching Hospital, Mohammed V University in Rabat, Rabat, Morocco.ORCID 0000-0002-5892-2863
Amale HassaniDepartment of Pediatrics, Mohammed V Military Teaching Hospital, Mohammed V University in Rabat, Rabat, Morocco.
Rachid AbilkassemDepartment of Pediatrics, Mohammed V Military Teaching Hospital, Mohammed V University in Rabat, Rabat, Morocco.ORCID 0000-0002-0418-7728

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

KBG syndrome is a rare autosomal dominant disorder characterised by developmental delay, characteristic facial features, macrodontia and skeletal anomalies, caused by mutations in the

Indexed as

Abnormalities, MultipleBone Diseases, DevelopmentalHearing LossIntellectual DisabilityRepressor ProteinsTooth AbnormalitiesChild, PreschoolFaciesHumansMaleMutationPhenotypeANKRD11 protein, humanRepressor ProteinsANKRD11Case ReportCraniofacial AbnormalitiesEpilepsyHearing LossKBG SyndromeMorroccoMutationNeurodevelopmental Disorders

Identifiers

PMID41809613
PMCPMC12969402

What OpenQuestion holds

Textmetadata
LicenceCC BY-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.