Evidence map›Paper›PMID 38028307›Full record

ArticleRadiology case reports2024

Dyke-Davidoff-Masson syndrome in an 8-year-old child: Report of a case.

Nourrelhouda Bahlouli, Fatima Chait, Khadija Laasri, Yahya El Harras, Nazik Allali, Latifa Chat, Siham El Haddad

Open access · goldAbstract readCase Reports
In one paragraph

Article in Radiology case reports, 2024. 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
0.4field-weighted citation impact, top 35% 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, 2 citations in OpenAlex.

  1. Dyke-Davidoff-Masson syndrome - A dainty spectrum with a diligent diagnosis.Journal of family medicine and primary care · 2024
    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 1 institution in 1 country.

Nourrelhouda BahlouliRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Fatima ChaitRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Khadija LaasriRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Yahya El HarrasRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Nazik AllaliRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Latifa ChatRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Siham El HaddadRadiology Department, Pediatric Teaching Hospital, Mohammed V University, Rabat, Morocco.
Mohammed V University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dyke-Davidoff-Masson syndrome (DDMS) is a rare entity. Few cases have been described in the literature. It can be symptomatic or asymptomatic. The clinical signs are very varied. Imaging is the key to diagnosis. Calvarial thickening, enlargement sinus, and cerebral hemiatrophy are suggestive signs. It is a cause of cerebral hemiatrophy and epilepsy. We report the clinical and radiological signs of this syndrome through a case of an 8-year-old male child treated for epilepsy. The importance of our article is to report a case diagnosed at an early age (8 years). Most studies report cases diagnosed in adults. MRI revealed pathognomonic signs of Dyke-Davidoff-Masson syndrome.

Indexed as

Calvarial thickeningChildrenDyke-Davidoff-Masson syndromeEpileptic seizuresHemi cerebral atrophyMRI

Identifiers

PMID38028307
PMCPMC10630757
OpenAlexW4388248062

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.