Evidence map›Paper›PMID 33088402›Full record

ArticleThe Pan African medical journal2020

[Sturge-Weber syndrome: about a case].

Meriem Doumiri, Mohamed Labied, Siham Salam, Dalal Laoudiyi, Kamilia Chbani, Lahcen Ouzidane

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

Article in The Pan African medical journal, 2020. 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
–field-weighted citation impact, top 84% 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. 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

6 authors at 1 institution in 1 country.

Meriem DoumiriService de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco.
Mohamed LabiedService de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco.
Siham SalamService de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco.
Dalal LaoudiyiService de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco.
Kamilia ChbaniService de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco.
Lahcen OuzidaneService de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco.
Hôpital 20 Août · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. It can cause two malformations: congenital facial capillary planar angioma and leptomeningal venous-capillary angioma (most often parieto-occipital homolateral angioma). Neuroimaging, in particular magnetic resonance imaging (MRI), plays an important role in the diagnosis, ideally before the occurrence of neuro-ocular complications. We report the case of a child in whom SWS was suspected based on facial angioma and pharmaco-resistant epilepsy.

Indexed as

ChildDrug Resistant EpilepsyHemangiomaHumansMagnetic Resonance ImagingMaleSturge-Weber SyndromeMRIplanar angiomaSturge-Weber

Identifiers

PMID33088402
PMCPMC7546018
OpenAlexW3048851223

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.