Evidence map›Paper›PMID 42529038›Full record

ArticleClinical case reports2026

Tuberous Sclerosis Complex (Bourneville-Pringle Disease) With Congenitally Right Solitary Kidney in a 14-Year-Old Male Adolescent.

Animaw Lingerew Dagnaw, Asressie Mamo Alemayehu, Gebre Hailu Dejen, Astarkew Alene Abejehu, Kindye Wale Kassie

Abstract read
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

5 authors.

Animaw Lingerew DagnawDepartment of Pediatrics and Child Health, School of Medicine, College of Medicine and Health Sciences Woldia University Ethiopia.ORCID https://orcid.org/0009-0000-2102-1001
Asressie Mamo AlemayehuDepartment of Dermatovenereology, School of Medicine, College of Medicine and Health Sciences Woldia University Woldia Ethiopia.
Gebre Hailu DejenDepartment of Radiology, School of Medicine, College of Medicine and Health Sciences Woldia University Woldia Ethiopia.
Astarkew Alene AbejehuDepartment of Internal Medicine, School of Medicine, College of Medicine and Health Sciences Woldia University Woldia Ethiopia.
Kindye Wale KassieDepartment of Ophthalmology, School of Medicine, College of Medicine and Health Sciences Woldia University Woldia Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coexistence of tuberous sclerosis complex (TSC) with a congenital solitary kidney is exceptionally rare and worsens prognosis. This combination increases the risk of renal failure, requiring meticulous monitoring, tailored surveillance, and renal preservation strategies. Early recognition, multidisciplinary care, and individualized management are essential to optimize outcomes in complex clinical scenarios.

Indexed as

angiomyolipomasautosomal dominantbourneville‐pringle diseasecongenital solitary kidneytuberous sclerosis complex (TSC)

Identifiers

PMID42529038
PMCPMC13415987

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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.