Evidence map›Paper›PMID 41589098›Full record

ArticleOxford medical case reports2026

A rare early-onset bilateral renal cysts, focal seizures in a 1-year-old male with tuberous sclerosis and No mutation identified.

Dana Salahat, Ramzi Mujahed, Mohanad Jaber, Mohammed Tahayneh, Nisreen Khalifa, Qais Alnjoom, Rani Sabra, Motasem Doudin, Raef Sabra, Ibraheem AbuAlrub

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

10 authors.

Dana SalahatMedical Student, Department of Clinical Medical Sciences, Faculty of Medicine and Health Sciences, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0007-0763-4662
Ramzi MujahedDepartment of Pediatrics Faculty of Medicine, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0006-9010-0129
Mohanad JaberHead of Clinical Medicine Department, Faculty of Medicine, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0008-3832-2319
Mohammed TahaynehHead of Basic Medicine Department, Faculty of Medicine, Palestine Polytechnic University, Hebron, Palestine.ORCID https://orcid.org/0009-0000-1485-3758
Nisreen KhalifaMedical Student, Department of Clinical Medical Sciences, Faculty of Medicine and Health Sciences, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0008-8020-0630
Qais AlnjoomMedical Student, Department of Clinical Medical Sciences, Faculty of Medicine and Health Sciences, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0007-3252-2128
Rani SabraMedical Student, Department of Clinical Medical Sciences, Faculty of Medicine and Health Sciences, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0005-8556-3084
Motasem DoudinDepartment of Pediatrics Nephrology, Faculty of Medicine, Hebron University, Hebron, Palestine.ORCID https://orcid.org/0009-0003-8003-1682
Raef SabraMedical Student, Department of Clinical Medical Sciences, Faculty of Medicine and Health Sciences, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0009-0004-2495-0665
Ibraheem AbuAlrubResearch and Teaching Assistant, Department of Clinical Medical Sciences, Faculty of Medicine, Palestine Polytechnic University, Hebron, P720, Palestine.ORCID https://orcid.org/0000-0002-2769-3033

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberous Sclerosis Complex (TSC) is a rare genetic disorder characterized by the development of benign tumors in multiple organs. This report presents an unusual case of early-onset renal cystic disease in a 1-year-old male with TSC, despite the absence of detectable mutations in the

Indexed as

case reportpolycystic kidneysubependymal giant cell astrocytomatuberous sclerosis complex

Identifiers

PMID41589098
PMCPMC12832028

What OpenQuestion holds

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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.