Evidence map›Paper›PMID 40402439›Full record

ArticleIndian journal of pediatrics2025

Neonatal Onset Seizures and Hypotonia Due to D-Bifunctional Protein Deficiency.

Sohier Yahia, Dina Ghozzy, Yahya Wahba, Zahraa Abdelmoneim

Erratum issuedAbstract readCase Reports
In one paragraph

Article in Indian journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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
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.

  1. Article
  2. One novelFrontiers in pediatrics · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Sohier YahiaDepartment of Pediatrics, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Dina GhozzyDepartment of Pediatrics, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Yahya WahbaDepartment of Pediatrics, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Zahraa AbdelmoneimDepartment of Pediatrics, Faculty of Medicine, Mansoura University, Mansoura, Egypt. hzahraa211@gmail.com.ORCID 0009-0005-3632-6410

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peroxisomal disorders (PDs) are a diverse group of inherited conditions arising from impaired function of a specific peroxisomal enzyme, metabolite transporter, or defect in the peroxisome biogenesis system. Peroxisomal D-bifunctional protein (DBP) deficiency is generally classified as a Zellweger-like syndrome. This disorder is caused by mutations in the HSD17B4 gene, and only a limited number of confirmed cases have been reported to date.The authors report case of a 6-mo-old female infant presenting with neonatal-onset intractable seizures, characteristic facial features, hypotonia, and progressive hepatomegaly. An acylcarnitine profile revealed elevated very long-chain fatty acids, prompting the initiation of a medium-chain triglyceride (MCT) formula. Remarkably, this treatment led to seizure control, improved muscle tone, and a reduction in liver size. Whole exome sequencing identified a homozygous missense mutation in the HSD17B4 gene (c.1444A>T).This case suggests that MCT-containing formulas may offer therapeutic potential in the treatment of D-bifunctional protein deficiency.

Indexed as

Muscle HypotoniaPeroxisomal Multifunctional Protein-2SeizuresFemaleHumansInfantMutation, MissenseTriglyceridesHSD17B4 protein, humanPeroxisomal Multifunctional Protein-2TriglyceridesHSD17B4Peroxisomal disorderSeizures

Identifiers

PMID40402439
PMCPMC12279582

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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.