Evidence map›Paper›PMID 42741765›Full record

ArticleOxford medical case reports2026

Normal neuroimaging in an infant with SUCLA2-related mitochondrial DNA depletion syndrome type 5: a case report of likely pathogenic variant.

Mohammad Obada Alsadi, Youssef Heikal, Farah Al-Hasani, Dana Al Khasawneh, Aia Nasab, Heba Hrizat, Fatema Almoustafa, Barah Hussain

Abstract readCase Reports
In one paragraph

Article in Oxford medical 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

8 authors.

Mohammad Obada AlsadiFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.ORCID https://orcid.org/0009-0004-8597-6164
Youssef HeikalDepartment of Otolaryngology, October 6 University, Giza, Egypt.
Farah Al-HasaniFaculty of medicine, Jordan University of Science and Technology, Irbid, Jordan.
Dana Al KhasawnehFaculty of medicine, Jordan University of Science and Technology, Irbid, Jordan.
Aia NasabFaculty of Medicine, University of Kalamoon, Deratiah, Syrian Arab Republic.
Heba HrizatHebron University, West Bank- Palestine.
Fatema AlmoustafaFaculty of Medicine, Al Andalus University for Medical Sciences, Tartus, Syrian Arab Republic.ORCID https://orcid.org/0009-0007-3624-4946
Barah HussainChildren's University Hospital, Damascus, Syrian Arab Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial DNA depletion syndrome type 5 (MTDPS5), caused by

Indexed as

EncephalomyopathymitochondrialSUCLA2WES

Identifiers

PMID42741765
PMCPMC13574277

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.