ArticleFrontiers in pediatrics2026
Epilepsy associated with
Article in Frontiers in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: To summarize the clinical characteristics, treatment response, and prognosis of epilepsy associated with Methods: Clinical and genetic data of six children diagnosed with SYNGAP1-related epilepsy at the Children's Hospital Affiliated to Zhengzhou University between November 2019 and February 2025 were retrospectively analyzed. Results: Among the six patients (four males and two females), the median age at seizure onset was 2 years and 8 months. All patients showed moderate to severe motor and language developmental delay, with prominent language impairment. Seizure types were heterogeneous, mainly including myoclonic seizures, eyelid myoclonia with or without absence seizures, myoclonic-atonic seizures, and absence seizure. Two patients had a history of febrile seizures, and four had identifiable seizure triggers. Electroencephalography revealed generalized or multifocal epileptiform discharges in all patients. Genetic analysis revealed that all six variants were Conclusions: Myoclonic seizures, absence seizures, and eyelid myoclonia are common in
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.