Evidence map›Paper›PMID 37090833›Full record

ArticleJournal of pediatric genetics2023

Carnitine-Acylcarnitine Translocase Deficiency Masked by Extreme Prematurity.

Kelli C Lund, Brian Scottoline, Brian K Jordan

Open access · greenAbstract read
In one paragraph

Article in Journal of pediatric genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 47% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

3 authors at 2 institutions in 1 country.

Kelli C LundDepartment of Pediatrics, Division of Neonatology, University of Utah, Salt Lake City, Utah, United States.ORCID 0000-0001-7154-9517
Brian ScottolineDivision of Neonatology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health & Science University, Portland, Oregon, United States.ORCID 0000-0003-0207-9624
Brian K JordanDivision of Neonatology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health & Science University, Portland, Oregon, United States.ORCID 0000-0002-1553-8503
Oregon Health & Science University · USUniversity of Utah · US

Funding

Oregon Clinical and Translational Research Institute KL2 SupplementKL2TR002370 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Catherine Lee Hough · 2017 to 2026
$10.1M
Trajectories of Lung Function in Extremely Premature InfantsK23HL144918 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JORDAN, BRIAN K · 2019 to 2023
$819k
NCATS NIH HHS KL2 TR002370NHLBI NIH HHS K23 HL144918
6 · The paper itself

Abstract

Carnitine-acylcarnitine translocase (CACT) deficiency is a rare disorder of long chain fatty acid oxidation with a very high mortality rate due to cardiomyopathy or multiorgan failure. We present the course of a very premature infant with early onset CACT deficiency complicated by multiple episodes of necrotizing enterocolitis, sepsis, and liver insufficiency, followed by eventual demise. The complications of prematurity, potentiated by the overlay of CACT deficiency, contributed to the difficulty of reaching the ultimate diagnosis of CACT deficiency.

Indexed as

CACTcarnitine-acylcarnitine translocase deficiencyprematurity

Identifiers

PMID37090833
PMCPMC10118704
OpenAlexW3133399800

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.