Evidence map›Paper›PMID 39814050›Full record

ReviewNeuropediatrics2025

Newborn with Refractory Seizures due to Hemimegalencephaly and Tuberous Sclerosis Complex: Case Report and Literature Review.

Mathies Rondagh, Linda S de Vries, Lotte E van der Meeren, Selma C Tromp, Cacha M P C D Peeters-Scholte, Menno J P Toirkens, Sylke J Steggerda

Abstract readCase ReportsReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Neuropediatrics, 2025. 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

7 authors.

Mathies RondaghDivision of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0009-0002-1715-093X
Linda S de VriesDivision of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands.
Lotte E van der MeerenDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Selma C TrompDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Cacha M P C D Peeters-ScholteDepartment of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Menno J P ToirkensDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
Sylke J SteggerdaDivision of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands.

Funding

Honours College Leids Universitair Medisch Centrum 240426Leids Universitair Fonds (LUF) and the Gratama Stichting 2023-10/W233029-2-GSLStrong Babies SB-JO-2023-15
6 · The paper itself

Abstract

Hemimegalencephaly (HME) is a rare congenital disorder that is initiated during embryonic development with abnormal growth of one hemisphere. Tuberous sclerosis complex (TSC), a genetic disorder, is rarely associated with HME.We present a case of a newborn with HME with a confirmed mutation in the

Indexed as

Drug Resistant EpilepsyHemimegalencephalySeizuresTuberous SclerosisElectroencephalographyHumansInfantInfant, NewbornMagnetic Resonance ImagingTuberous Sclerosis Complex 1 ProteinTSC1 protein, humanTuberous Sclerosis Complex 1 Protein

Identifiers

PMID39814050
PMCPMC11932765

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.