Evidence map›Paper›PMID 41079045›Full record

ArticleCase reports in pediatrics2025

Prolidase Deficiency Presenting With Pulmonary Arteriovenous Malformations and Seizures: Report of Two Cases From Iran.

Ali Pajouhi, Rouhollah Rohani, Vahid Ziaee, Mohammad Shahrooei, Zeinab Paymani, Bahar Amiri, Mohammadreza Modaresi

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports 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

7 authors.

Ali PajouhiStudent Research Committee, Lorestan University of Medical Sciences, Khorramabad, Iran.ORCID https://orcid.org/0000-0002-5445-4951
Rouhollah RohaniPediatric Respiratory and Sleep Medicine Research Center, Children's Medical Center, Pediatric Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0009-0005-4555-268X
Vahid ZiaeeChildren's Medical Center, Pediatric Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0003-4648-3573
Mohammad ShahrooeiClinical and Diagnostic Immunology, Department of Microbiology, Immunology, and Transplantation, KU Leuven, Leuven 3000, Belgium.ORCID https://orcid.org/0000-0002-4974-3441
Zeinab PaymaniDepartment of Nuclear Medicine, Children's Medical Center, Pediatric Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-7009-5127
Bahar AmiriStudent Research Committee, Lorestan University of Medical Sciences, Khorramabad, Iran.ORCID https://orcid.org/0009-0008-1842-1520
Mohammadreza ModaresiPediatric Respiratory and Sleep Medicine Research Center, Children's Medical Center, Pediatric Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-9625-5184

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prolidase deficiency (PD) is a rare autosomal recessive metabolic disorder caused by pathogenic variants in the

Indexed as

AVMsgenetic disordersIranprolidase deficiencypulmonary arteriovenous malformationsrare diseasesseizure

Identifiers

PMID41079045
PMCPMC12510767

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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.