Evidence map›Paper›PMID 40217411›Full record

ReviewActa epileptologica2025

Advances in genetic developmental and epileptic encephalopathies with movement disorders.

Meng Yuan, Xiaoqian Wang, Zuozhen Yang, Huan Luo, Jing Gan, Rong Luo

Abstract readReview
In one paragraph

Review in Acta epileptologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

6 authors.

Meng Yuan *Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Xiaoqian Wang *Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Zuozhen YangCipher Gene LLC, Beijing, 100089, China.
Huan LuoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Jing GanDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China. gordonrachel@163.com.ORCID http://orcid.org/0000-0001-5255-6324
Rong LuoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China. 1109329811@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic developmental and epileptic encephalopathies (DEE) are often associated with movement disorders. Accurate identification and classification of movement disorders are essential for management of these diseases. In this review, we describe the characteristics of various movement disorders associated with DEE and summarize the distribution of common DEE-related gene mutations reported in previous studies, aiming to provide references for the diagnosis and treatment of these disorders.

Indexed as

Developmental and epileptic encephalopathiesGeneticMovement disorders

Identifiers

PMID40217411
PMCPMC11960234

What OpenQuestion holds

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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.