Evidence map›Paper›PMID 33671521›Full record

ArticleChildren (Basel, Switzerland)2021

Perspective on Similarities and Possible Overlaps of Congenital Disease Formation-Exemplified on a Case of Congenital Diaphragmatic Hernia and Neuroblastoma in a Neonate.

Zihe Huo, Remo Bilang, Benedikt Brantner, Nicolas von der Weid, Stefan G Holland-Cunz, Stephanie J Gros

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2021. 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
0.1field-weighted citation impact, top 56% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

6 authors at 2 institutions in 1 country.

Zihe HuoDepartment of Pediatric Surgery, University Children's Hospital Basel, 4031 Basel, Switzerland.
Remo BilangDepartment of Pediatric Surgery, University Children's Hospital Basel, 4031 Basel, Switzerland.
Benedikt BrantnerDepartment of Pediatric Surgery, University Children's Hospital Basel, 4031 Basel, Switzerland.
Nicolas von der WeidDepartment of Clinical Research, University of Basel, 4001 Basel, Switzerland.
Stefan G Holland-CunzDepartment of Pediatric Surgery, University Children's Hospital Basel, 4031 Basel, Switzerland.
Stephanie J GrosDepartment of Pediatric Surgery, University Children's Hospital Basel, 4031 Basel, Switzerland.
University Children’s Hospital Basel · CHUniversity of Basel · CH

Funding

China Scholarship Council 201706920049
6 · The paper itself

Abstract

The coincidence of two rare diseases such as congenital diaphragmatic hernia (CDH) and neuroblastoma is exceptional. With an incidence of around 2-3:10,000 and 1:8000 for either disease occurring on its own, the chance of simultaneous presentation of both pathologies at birth is extremely low. Unfortunately, the underlying processes leading to congenital malformation and neonatal tumors are not yet thoroughly understood. There are several hypotheses revolving around the formation of CDH and neuroblastoma. The aim of our study was to put the respective hypotheses of disease formation as well as known factors in this process into perspective regarding their similarities and possible overlaps of congenital disease formation. We present the joint occurrence of these two rare diseases based on a patient presentation and immunochemical prognostic marker evaluation. The aim of this manuscript is to elucidate possible similarities in the pathogeneses of both disease entities. Discussed are the role of toxins, cell differentiation, the influence of retinoic acid and NMYC as well as of hypoxia. The detailed discussion reveals that some of the proposed pathophysiological mechanisms of both malformations have common aspects. Especially disturbances of the retinoic acid pathway and NMYC expression can influence and disrupt cell differentiation in either disease. Due to the rarity of both diseases, interdisciplinary efforts and multi-center studies are needed to investigate the reasons for congenital malformations and their interlinkage with neonatal tumor disease.

Indexed as

AQP1CDHdifferentiationhypoxianeuroblastomaNMYCorphan diseasepediatric surgeryrare diseaseretinoic acid pathway

Identifiers

PMID33671521
PMCPMC7926624
OpenAlexW3131468132

What OpenQuestion holds

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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.