Evidence map›Paper›PMID 32734401›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2020

Cleidocranial dysplasia, a rare skeletal disorder with failure of the cranial closure: case-based update.

Laryssa C Azevedo Almeida, Franklin B Faraj de Lima, Hamilton Matushita, Marcelo M Valença, Tamireis L Ferreira Castro, Rafael N de Mendonça

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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  3. Review
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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.

Laryssa C Azevedo AlmeidaCentre for Neurology and Neurosurgery at Santa Casa de Misericórdia de Belo Horizonte, Belo Horizonte, Minas Gerais, Brazil. laryssazevedo@hotmail.com.ORCID 0000-0002-9002-7906
Franklin B Faraj de LimaCentre for Neurology and Neurosurgery at Santa Casa de Misericórdia de Belo Horizonte, Belo Horizonte, Minas Gerais, Brazil.
Hamilton MatushitaDivision of Neurological Surgery, University of São Paulo, Sao Paulo, Brazil.
Marcelo M ValençaNeurology and Neurosurgery Unit, Department of Neuropsychiatry, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Tamireis L Ferreira CastroUniversity Center of Belo Horizonte, Belo Horizonte, Minas Gerais, Brazil.
Rafael N de MendonçaUniversity Center of Belo Horizonte, Belo Horizonte, Minas Gerais, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimCleidocranial dysplasia is a rare disorder of skeletal development that mainly promotes, among other malformations, inadequate development of clavicles and failure in cranial closure. In this affection, the role of neurosurgery in addressing cranial defects is rarely discussed. MATERIAL AND

methodsWe conducted an extensive review of the literature using the PubMed database, giving a greater focus to publications in the field of neurosurgery. Additionally, we report a case of a 2-year-old female child with cleidocranial dysplasia.

resultsIn our review, we encountered several cases of orthodontic implications but a few cases on cranial defect approach.

conclusionThe articles present literature that is unanimous on the recommendation of expectant conduct in children since the cranial block can occur spontaneously, even if the delayed form. In our approach, we opted for an expected strategy concerning the cranial defect, using a helmet made for brain protection. We also made the referral for multidisciplinary monitoring of pediatrics, neuropediatrics, ophthalmology, dentistry, and orthopedics.

Indexed as

Cleidocranial DysplasiaChild, PreschoolFemaleHead Protective DevicesHumansSkullCleidocranial dysostosisCraniofacial abnormalitiesRUNX2 mutationSkeletal disorders

Identifiers

What OpenQuestion holds

Textmetadata
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.