Evidence map›Paper›PMID 34322265›Full record

ArticleClinical case reports2021

3-Hydroxyisobutyryl-CoA hydrolase deficiency in an infant with developmental delay and high anion gap acidosis.

Hedyeh Saneifard, Asieh Mosallanejad, Aida Fallahzadeh, Ali Sheikhy

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2021. 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
0.4field-weighted citation impact, top 41% 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, 3 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

4 authors at 3 institutions in 1 country.

Hedyeh SaneifardMofid Children's Hospital Shahid Beheshti University of Medical Sciences Tehran Iran.
Asieh MosallanejadImam Hosein Medical Center Shahid Beheshti University of Medical Sciences Tehran Iran.
Aida FallahzadehResearch Department Tehran Heart Center Tehran University of Medical Sciences Tehran Iran.
Ali SheikhyResearch Department Tehran Heart Center Tehran University of Medical Sciences Tehran Iran.ORCID https://orcid.org/0000-0002-0358-4406
Iran University of Medical Sciences · IRImam Hossein Hospital · IRShahid Beheshti University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the rarity of this disorder, paying attention to diagnostic clues is important. Low valine formula seems to be effective in improvement of patient's symptoms. Prevention of consanguineous marriage is the best way to prevent this disease.

Indexed as

3‐hydroxyisobutyryl‐CoAacidosisdevelopmental disabilitydystonia

Identifiers

PMID34322265
PMCPMC8299097
OpenAlexW3183894972

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.