Evidence map›Paper›PMID 38468680›Full record

ArticleSurgical neurology international2024

Fontanellar bone - A rarity in pediatric cranial abnormalities.

Ibrahim H Alahmed, Abdulelah S Almousa, Abdulsalam Aleid

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Surgical neurology international, 2024. 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
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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

3 authors at 1 institution in 2 countries.

Ibrahim H AlahmedAlmoosa Specialist Hospital, Al-Ahsa, Saudi Arabia.
Abdulelah S AlmousaDepartment of Neurosurgery, College of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia.
Abdulsalam AleidDepartment of Neurosurgery, College of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia.
King Faisal University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Fontanelles, membranous gaps in the infant skull, are integral for accommodating the expansion of the skull by the growing brain postnatally. The anterior fontanelle, situated at the frontal-parietal bone intersection, typically closes gradually within the first two years. Fontanellar bone, an exceedingly rare ossification anomaly of the anterior fontanelle, clinically mimics craniosynostosis. Case Description: We present the case of a 22-day-old male with an almost closed anterior fontanelle who underwent evaluation. Prenatal and postnatal history were unremarkable. Physical examination revealed a well-nourished infant with a nearly closed fontanelle but no other anomalies. The initial diagnosis was craniosynostosis; however, a head computed tomography scan revealed fontanellar bone. Consequently, a conservative management approach with regular follow-ups was adopted. Conclusion: This case provides valuable insights into fontanellar bone, emphasizing its consideration in differential diagnoses for almost closed anterior fontanelles. The report aims to enhance awareness and understanding of this rare condition, promoting accurate diagnosis and optimal patient outcomes.

Indexed as

Case reportCranial abnormalitiesCraniosynostosisFontanellar bone

Identifiers

PMID38468680
PMCPMC10927169
OpenAlexW4392357796

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.