Evidence map›Paper›PMID 41341108›Full record

ArticleFrontiers in pediatrics2025

Case Report: Lethal neonatal form of CPT II deficiency in consecutive pregnancies: fetal-neonatal characteristics, biochemical and molecular review.

Y Y Tan, K G Tewani, A J Anand, C X Kong, V S Rajadurai, S Chandran

Abstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 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

6 authors.

Y Y TanDepartment of Neonatology, KK Women's and Children's Hospital, Singapore, Singapore.
K G TewaniPediatric Obstetrics & Gynecology Clinical Program, Duke NUS Medical School, Singapore, Singapore.
A J AnandDepartment of Neonatology, KK Women's and Children's Hospital, Singapore, Singapore.
C X KongDepartment of Neonatology, KK Women's and Children's Hospital, Singapore, Singapore.
V S RajaduraiDepartment of Neonatology, KK Women's and Children's Hospital, Singapore, Singapore.
S ChandranDepartment of Neonatology, KK Women's and Children's Hospital, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carnitine palmitoyltransferase II (CPT II) deficiency is a rare inherited disorder of mitochondrial oxidation of long-chain fatty acids (LCFA). Carnitine is the sole carrier of LCFA, which is transferred to the cellular mitochondria for

Indexed as

carnitineCPT II deficiencyfatty acid oxidationpolycystic kidneysventriculomegaly

Identifiers

PMID41341108
PMCPMC12669159

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.