Evidence map›Paper›PMID 39742135›Full record

ArticleCase reports in medicine2024

Congenital Nasal Bones Agenesis: Report of a Rare Malformation.

Monica Russo, Chiara Ferrecchi, Silvia Rebella, Valeria Capra, Franco Ameli, Mattia Pacetti, Maria Francesca Di Feo, Pierangela De Biasio, Cesare Arioni

Abstract readCase Reports
In one paragraph

Article in Case reports in medicine, 2024. 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
–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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Monica RussoOperative Unit of Neonatology, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.ORCID https://orcid.org/0000-0002-7589-426X
Chiara FerrecchiDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Sciences (DINOGMI), University of Genoa, Genoa, Italy.
Silvia RebellaDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Sciences (DINOGMI), University of Genoa, Genoa, Italy.
Valeria CapraGenomics and Clinical Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Franco AmeliOtorhinolaringology Department, Casa di Cura Villa Montallegro, Genoa, Italy.
Mattia PacettiDepartment of Neurosurgery, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Maria Francesca Di FeoGenomics and Clinical Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Pierangela De BiasioHead Fetal Medicine Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Cesare ArioniOperative Unit of Neonatology, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital arhinia and hyporhinia are rare facial anomalies whose knowledge usually comes from case reports. The severity of each case described in literature is variable; it also depends on associated malformations too. Since the newborns are obligate nasal breathers, babies with arhinia or hyporhinia usually have respiratory distress and need airway stabilization. In addition, most of these children present difficulties in feeding and this impairment must be managed early. We describe an unusual case of partial congenital arhinia, the baby did not have other anomalies or any specific complication such as respiratory and feeding issues, so the major problem was the aesthetic and psychological issues for the family. Even if the neonatal course was uncomplicated, a coordinated approach of the pediatrician with the pediatric otolaryngologist, the geneticists and the neurosurgeons was necessary because the management of these malformations is always very complex; due to the lack of reports described in literature, an univocal management and also the best timing and technique for reconstructive surgery are still not defined.

Indexed as

agenesisarhiniagenetichyporhiniamalformationnasal bonesneonatology

Identifiers

PMID39742135
PMCPMC11685316

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.