Evidence map›Paper›PMID 37455866›Full record

ArticleThe Pan African medical journal2023

Congenital surfactant protein B (SP-B) deficiency: a case report.

Fatma Khalsi, Maha Chaabene, Manel Ben Romdhane, Ines Trabelsi, Samia Hamouda, Alix de Becdelièvre, Khedija Boussetta

Open access · greenAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in The Pan African medical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 2 countries.

Fatma KhalsiPediatrics Department B, Children's Hospital of Tunis, Tunis, Tunisia.
Maha ChaabenePediatrics Department B, Children's Hospital of Tunis, Tunis, Tunisia.
Manel Ben RomdhanePediatrics Department B, Children's Hospital of Tunis, Tunis, Tunisia.
Ines TrabelsiPediatrics Department B, Children's Hospital of Tunis, Tunis, Tunisia.
Samia HamoudaPediatrics Department B, Children's Hospital of Tunis, Tunis, Tunisia.
Alix de BecdelièvreDepartment of Genetic, Henri Mondor Hospital, Genetic_Mondor, Public Assistance of the Hospitals of Paris, Delattre de Tassigny, Creteil, France.
Khedija BoussettaPediatrics Department B, Children's Hospital of Tunis, Tunis, Tunisia.
Children's Hospital · TNParis-Est Sup · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incapacity to synthesize certain components of pulmonary surfactant causes a heterogeneous group of rare respiratory diseases called genetic disorders of surfactant dysfunction. We report a female full-term infant with neonatal respiratory distress of early onset due to inherited SP-B deficiency. The infant failed oxygen weaning at multiple trials. Chest computed tomography was performed on the 29

Indexed as

Respiratory Distress Syndrome, NewbornDNAFemaleHumansInfantInfant, NewbornLung Diseases, InterstitialPulmonary Alveolar ProteinosisPulmonary Surfactant-Associated Protein BReceptors, FcSurface-Active AgentsDNAIgA receptorPulmonary Surfactant-Associated Protein BReceptors, FcSurface-Active Agentscase reportgeneticslung diseaseneonatal respiratory distressSP-B deficiency

Identifiers

PMID37455866
PMCPMC10349626
OpenAlexW4384493351

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.