Evidence map›Paper›PMID 36328362›Full record

ArticleBMJ case reports2022

Infant with Loeys-Dietz syndrome treated for febrile status epilepticus with COVID-19 infection: first reported case of febrile status epilepticus and focal seizures in a patient with Loeys-Dietz syndrome and review of literature.

Asra Akbar, Sharjeel Ahmad, Sean Creeden, Huan Huynh

Open access · greenAbstract readCase Reports
In one paragraph

Article in BMJ case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. The genetics of hyper IgE syndromes.Frontiers in immunology · 2025
    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

4 authors at 3 institutions in 1 country.

Asra AkbarDepartment of Pediatric Neurology, UICOMP, Peoria, Illinois, USA aakbar1@uic.edu.ORCID http://orcid.org/0000-0002-0100-4463
Sharjeel AhmadDepartment of Internal Medicine, Section of Infectious Diseases, University of Illinois College of Medicine at Peoria, Peoria, Illinois, USA.ORCID http://orcid.org/0000-0002-4152-2337
Sean CreedenDepartment of Radiology, University of Illinois College of Medicine at Peoria, Peoria, Illinois, USA.
Huan HuynhIllinois Neurological Institute, Peoria, Illinois, USA.
Illinois College · USPeoria campus of the University of Illinois System · USUniversity of Illinois Urbana-Champaign · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loeys-Dietz syndrome (LDS) is a rare, autosomal dominant multisystem disorder that is caused by mutations of transforming growth factor-β receptors. Mutations in

Indexed as

COVID-19Loeys-Dietz SyndromeStatus EpilepticusChildHumansInfantReceptors, Transforming Growth Factor betaSeizuresReceptors, Transforming Growth Factor betaEpilepsy and seizuresGenetic screening / counsellingInfectious diseasesNeuro geneticsNeuroimaging

Identifiers

PMID36328362
PMCPMC9639018
OpenAlexW4308026784

What OpenQuestion holds

Textmetadata
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.