Evidence map›Paper›PMID 41283373›Full record

ArticlePediatric reports2025

Is Beta Ketothiolase Deficiency an Uncommon Disease or an Unsuspected Diagnosis? The Role of Genetic Biochemistry Approaches in Metabolic Acidosis.

Luis D Campos-Acevedo, Joel Arenas-Estala, Marisol Ibarra-Ramírez, Graciela A López-Uriarte, María C Ruíz-Herrera, Marcelo Rodríguez-Rivera, Laura E Martínez-de-Villarreal

Abstract readCase Reports
In one paragraph

Article in Pediatric reports, 2025. 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

7 authors.

Luis D Campos-AcevedoGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.
Joel Arenas-EstalaGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.ORCID 0000-0003-4312-0910
Marisol Ibarra-RamírezGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.ORCID 0000-0002-3875-4532
Graciela A López-UriarteGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.
María C Ruíz-HerreraGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.
Marcelo Rodríguez-RiveraGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.
Laura E Martínez-de-VillarrealGenetics Department, Hospital Universitario "Dr. José Eleuterio González" and Medicine Faculty, Autonomous University of Nuevo León, Monterrey 64460, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beta ketothiolase deficiency is a hereditary metabolic disorder caused by the pathogenic variants of the

Indexed as

isoleucine metabolismketolysis defectsmetabolic acidemia

Identifiers

PMID41283373
PMCPMC12641768

What OpenQuestion holds

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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.