Evidence map›Paper›PMID 31073471›Full record

ArticleJournal of pediatric intensive care2018

A Case of Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Presenting with Severe Acidosis in a 14-Month-Old Female: Evidence for Pathogenicity of a Point Mutation in the

Daniel J Zheng, Michael Hooper, Michele Spencer-Manzon, Richard W Pierce

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of pediatric intensive care, 2018. 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
–field-weighted citation impact, top 91% 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, 5 citations in OpenAlex.

  1. [Succinyl CoA:3 oxoacid CoA transferase deficiency: A case report].Revista medica del Instituto Mexicano del Seguro Social · 2023
    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

4 authors at 1 institution in 1 country.

Daniel J ZhengDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, United States.
Michael HooperDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, United States.
Michele Spencer-ManzonDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, United States.
Richard W PierceDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, United States.
Yale University · US

Funding

YALE PEDIATRIC BASIC SCIENCE TRAINING PROGRAMT32HD068201 · NICHD · YALE UNIVERSITY · PI EGAN, MARIE E · 2011 to 2015
$1.3M
NICHD NIH HHS T32 HD068201
6 · The paper itself

Abstract

We describe a case of succinyl-CoA:3-oxoacid CoA transferase (SCOT) deficiency in an otherwise healthy 14 month-old female. She presented with lethargy, tachypnea, and hyperpnea with hypoglycemia and a severe anion gap metabolic acidosis. Early management included correction of the acidosis and metabolic support with dextrose and insulin. Inborn errors of metabolism are rare outside the neonatal period. However, SCOT deficiency may present at older ages. Maintaining a high index of suspicion, immediate transfer to a pediatric intensive care unit, and prompt metabolic support are key to achieving a favorable outcome.

Indexed as

ketoacidosisOXCT1 genesuccinyl-coA:3-oxoacid CoA transferase deficiency

Identifiers

PMID31073471
PMCPMC6260335
OpenAlexW2736373621

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.