Evidence map›Paper›PMID 40794016›Full record

ReviewEpileptic disorders : international epilepsy journal with videotape2025

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature.

D Kapoor, S Sharma, A Kaminska, R Nabbout, N Chemaly, M Schiff, P De Lonlay, M Eisermann

Abstract readReview
In one paragraph

Review in Epileptic disorders : international epilepsy journal with videotape, 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

8 authors.

D KapoorNeurology Division, Department of Pediatrics, Lady Hardinge Medical College and Associated Kalawati Saran Children's Hospital, New Delhi, India.
S SharmaDivision of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada.
A KaminskaClinical Neurophysiology, Necker Enfants Malades University Hospital, AP-HP, University of Paris Cité, Paris, France.
R NabboutReference Center for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades University Hospital, APHP, ERN EPICARE, and University Paris Cité, Paris, France.
N ChemalyReference Center for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades University Hospital, APHP, ERN EPICARE, and University Paris Cité, Paris, France.
M SchiffReference Center for Inborn Errors of Metabolism, Necker University Hospital, APHP and University of Paris Cité, Paris, France.ORCID https://orcid.org/0000-0001-8272-232X
P De LonlayReference Center of Inherited Metabolic Diseases, Necker-Enfants-Malades University Hospital, APHP and University of Paris Cité, Institut Imagine, Filière G2M, MetabERN, Paris, France.
M EisermannClinical Neurophysiology, Necker Enfants Malades University Hospital, AP-HP, University of Paris Cité, Paris, France.ORCID https://orcid.org/0000-0003-3634-2101

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although inborn errors of metabolism (IEM) are a rare cause of epilepsy, seizures are a common presentation in these disorders. Seizures in IEM are frequently refractory to conventional anti-seizure medication and might warrant initiation of specific treatments based on vitamins or dietary modifications or provision of alternative substrates (to bypass a block). In most IEMs, seizures present with variable and non-specific semiology and EEG findings. Nevertheless, certain distinctive electro-clinical features might suggest an underlying IEM and even point towards the etiology. Even though biochemical and genetic tests will confirm the definitive diagnosis, EEG has the great advantage of being rapidly available, before the results of these tests. This article aims to describe through a literature review, illustrated by videos and EEGs from personal cases, seizures, and EEG patterns in IEM. We will focus on distinctive electro-clinical features that may help the clinician to establish an appropriate diagnosis allowing a prompt and specific treatment in order to improve outcome.

Indexed as

ElectroencephalographyMetabolism, Inborn ErrorsSeizuresAdolescentChildChild, PreschoolDiagnosis, DifferentialHumansInfantInfant, NewbornEEGEtiology: metabolicinborn errors of metabolismLocalization: not applicablePhenomenology: multipleseizuresSyndrome: not applicable

Identifiers

PMID40794016
PMCPMC12998520

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.