Evidence map›Paper›PMID 40217346›Full record

ReviewActa epileptologica2025

Focal cortical dysplasia type II: review of neuropathological manifestations and pathogenetic mechanisms.

Yubao Fang, Yaqian Zhang, Tiancai Huang, Shengyu Yang, Yinchao Li, Liemin Zhou

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Yubao Fang *Department of Neurology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, 518107, China.
Yaqian Zhang *Department of Neurology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, 518107, China.
Tiancai HuangDepartment of Neurology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, 518107, China.
Shengyu YangDepartment of Neurology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, 518107, China.
Yinchao LiDepartment of Neurology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, 518107, China.
Liemin ZhouDepartment of Neurology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, 518107, China. zhoulm@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-9387-7244

Funding

Innovative Research Group Project of the National Natural Science Foundation of China LMZ 82071447,82371456Science, Technology and Innovation Commission of Shenzhen Municipality LMZ JCYJ20220818102007015
6 · The paper itself

Abstract

Focal cortical dysplasia (FCD) is an important cause of intractable epilepsy, with FCD type II (FCD II) being the most common subtype. FCD II is characterized by cortical dyslamination accompanied by dysmorphic neurons (DNs). Identifying the molecular alterations and targetable biomarkers is pivotal for developing therapies. Here, we provide a detailed description of the neuropathological manifestations of FCD II, including morphological alterations and immunophenotypic profiles, indicating that abnormal cells exhibit a diverse spectrum of mixed differentiation states. Furthermore, we summarize current research on the pathogenetic mechanisms, indicating that gene mutations, epigenetic alterations, cortical developmental protein disturbances, inflammatory processes, and extrinsic damages may lead to abnormal neuronal proliferation and migration, thereby contributing to the emergence and progression of FCD II. These findings not only enhance our understanding of the pathogenesis of FCD II but also offer new directions for clinical diagnosis and treatment. Future research should further explore the interactions among these factors and employ multidisciplinary approaches to advance our understanding of FCD II.

Indexed as

Abnormal differentiationEpigenetic alterationsFocal cortical dysplasiaGene mutations

Identifiers

PMID40217346
PMCPMC11960379

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.