Evidence map›Paper›PMID 42042759›Full record

ArticleNeurology international2026

Long-Term Follow-Up of a Patient with a Novel Homozygous

Buşra Kasap, Dilek Uludağ Alkaya, Nilay Güneş, Salih Türk, Barış Korkmaz, Beyhan Tüysüz

Abstract readCase Reports
In one paragraph

Article in Neurology international, 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.

Buşra KasapDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Turkey.ORCID 0000-0002-4827-4225
Dilek Uludağ AlkayaDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Turkey.
Nilay GüneşDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Turkey.ORCID 0000-0002-7787-3630
Salih TürkDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Turkey.ORCID 0009-0002-0190-9139
Barış KorkmazDepartment of Neurology, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Turkey.
Beyhan TüysüzDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Turkey.

Funding

Istanbul University-Cerrahpaşa TOA-2019-33466
6 · The paper itself

Abstract

BACKGROUND/

objectivesSevere neurodevelopmental disorders caused by homozygous

methodsWe conducted a 15-year clinical evaluation of a girl who initially presented at 10 years of age. The genetic etiology was investigated using exome sequencing.

resultsThe patient had a profound intellectual disability, severe expressive language delay, and infantile-onset epilepsy. She also had microcephaly, achieved independent walking at age 7 and had speech limited to only two words at admission. A novel homozygous frameshift variant, c.2096del (p.Cys699Serfs*22), in

conclusions

Indexed as

ASTN1exome sequencingmicrocephalyneurodevelopmental disorder

Identifiers

PMID42042759
PMCPMC13119278

What Socratic holds

Textmetadata
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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.