Evidence map›Paper›PMID 39119448›Full record

ArticleMolecular syndromology2024

Two Sibling Cases of Spastic Paraplegia-45 with a Novel Pathogenic Variant in

Rojan İpek, Mustafa Kömür, Meltem Çobanoğulları Direk, Sevcan Tuğ Bozdoğan, Çetin Okuyaz

Abstract read
In one paragraph

Article in Molecular syndromology, 2024. 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

5 authors.

Rojan İpekDepartment of Pediatric Neurology, Dicle University, Diyarbakır, Turkey.
Mustafa KömürDepartment of Pediatric Neurology, Mersin University, Mersin, Turkey.
Meltem Çobanoğulları DirekDepartment of Pediatric Neurology, Mersin University, Mersin, Turkey.
Sevcan Tuğ BozdoğanDepartment of Medical Genetics, Cukurova University, Adana, Turkey.
Çetin OkuyazDepartment of Pediatric Neurology, Mersin University, Mersin, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hereditary spastic paraplegia ( Case Presentation: Two sisters, aged 8 and 4, exhibited delayed motor development since early childhood. They also experienced learning difficulties, dysarthric speech, ataxia, nystagmus, strabismus, and spasticity in their extremities. Additionally, brisk deep tendon reflexes were observed in their upper and lower limbs, and they exhibited positive pathological reflexes. Whole-exome sequencing identified a previously unidentified homozygous mutation in the Discussion/Conclusion: To the best of our knowledge, we report the first case of a patient with coexistence of the

Indexed as

Hereditary spastic paraplegiaInfantRYR1 geneSPG45

Identifiers

PMID39119448
PMCPMC11305657

What OpenQuestion holds

Textmetadata
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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.