Evidence map›Paper›PMID 42311771›Full record

ArticleClinical case reports2026

Familial SCN1A-Related Epilepsy in Palestinian Siblings: Challenges of Genetic Testing in Resource-Limited Settings: A Case Report.

Anwar Abu Hetta, Raghad S Razem, Shams Shahateet, Bushra Kh Pujee, Amal M Shawabka, Bara M AbuIrayyeh

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2026. 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

6 authors.

Anwar Abu HettaFaculty of Medicine Palestine Polytechnic University Hebron Palestine.
Raghad S RazemFaculty of Medicine Palestine Polytechnic University Hebron Palestine.
Shams ShahateetFaculty of Medicine Palestine Polytechnic University Hebron Palestine.
Bushra Kh PujeeFaculty of Medicine Palestine Polytechnic University Hebron Palestine.
Amal M ShawabkaFaculty of Medicine Palestine Polytechnic University Hebron Palestine.ORCID https://orcid.org/0000-0003-3125-5965
Bara M AbuIrayyehFaculty of Medicine Palestine Polytechnic University Hebron Palestine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SCN1A-related epilepsy may present in siblings with febrile and afebrile seizures. In resource-limited settings, diagnosis relies heavily on clinical recognition and established criteria. Early identification and avoidance of sodium channel blockers are critical, while genetic testing, when available, supports diagnosis and family counseling.

Indexed as

autosomal dominant epilepsycase reportDravet syndromeGEFS+resource‐limited settingsSCN1A mutationSCN1A‐related epilepsy

Identifiers

PMID42311771
PMCPMC13269654

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Registered trials

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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.