Evidence map›Paper›PMID 37805811›Full record

ArticleEpilepsia open2024

Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants.

Norman Panza, Claudia Bianchini, Valentina Cetica, Simona Balestrini, Carmen Barba, Anna Rita Ferrari, Davide Mei, Lucio Parmeggiani, Elena Parrini, Renzo Guerrini

Open access · goldAbstract read
In one paragraph

Article in Epilepsia open, 2024. 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
0.6field-weighted citation impact, top 23% of its field
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, 2 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Norman PanzaNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0009-0004-4110-6781
Claudia BianchiniNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0002-7144-785X
Valentina CeticaNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0001-8549-4158
Simona BalestriniNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0001-5639-1969
Carmen BarbaNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0001-5445-5842
Anna Rita FerrariIRCCS Stella Maris, Calambrone, Pisa, Italy.ORCID 0000-0002-5397-6184
Davide MeiNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0001-6790-6251
Lucio ParmeggianiDepartment of Pediatric Neurology, Bolzano Hospital, Bolzano, Italy.ORCID 0000-0002-2556-5601
Elena ParriniNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0001-8933-7694
Renzo GuerriniNeuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID 0000-0002-7272-7079
Meyer Children's Hospital · ITFondazione Stella Maris · ITOspedale di Bolzano · IT

Funding

Fondazione Cassa di Risparmio di FirenzeMinistry of University and Research (MUR), National Recovery and Resilience Plan (NRRP) PE0000006Tuscany Region Call for Health 2018 DECODE-EE
6 · The paper itself

Abstract

Biallelic CNTNAP2 variants have been associated with Pitt-Hopkins-like syndrome. We describe six novel and one previously reported patients from six independent families and review the literature including 64 patients carrying biallelic CNTNAP2 variants. Initial reports highlighted intractable focal seizures and the failure of epilepsy surgery in children, but subsequent reports did not expand on this aspect. In all our patients (n = 7), brain MRI showed bilateral temporal gray/white matter blurring with white matter high signal intensity, more obvious on the T2-FLAIR sequences, consistent with bilateral temporal lobe dysplasia. All patients had focal seizures with temporal lobe onset and semiology, which were recorded on EEG in five, showing bilateral independent temporal onset in four. Epilepsy was responsive to anti-seizure medications in two patients (2/7, 28.5%), and pharmaco-resistant in five (5/7, 71.5%). Splice-site variants identified in five patients (5/7, 71.5%) were the most common mutational finding. Our observation expands the phenotypic and genetic spectrum of biallelic CNTNAP2 alterations focusing on the neuroimaging features and provides evidence for an elective bilateral anatomoelectroclinical involvement of the temporal lobes in the associated epilepsy, with relevant implications on clinical management.

Indexed as

EpilepsyEpilepsy, Temporal LobeChildElectroencephalographyHumansMembrane ProteinsNerve Tissue ProteinsSeizuresTemporal LobeCNTNAP2 protein, humanMembrane ProteinsNerve Tissue ProteinsCNTNAP2focal cortical dysplasiagenetic epilepsytemporal lobe epilepsy

Identifiers

PMID37805811
PMCPMC10839365
OpenAlexW4387432865

What OpenQuestion holds

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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 OpenQuestion graph.