Evidence map›Paper›PMID 23443469›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2013

Sprengel's deformity and spinal dysraphism: connecting the shoulder and the spine.

J van Aalst, J S H Vles, I Cuppen, D A Sival, E H Niks, L W Van Rhijn, M A M Van Steensel, E M J Cornips

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2013. 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, top 87% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

8 authors at 4 institutions in 1 country.

J van AalstDepartment of Neurosurgery, Maastricht University Medical Center, Oxfordlaan 10, 6229, EV, Maastricht, The Netherlands. j.van.aalst@mumc.nl.
J S H VlesDepartment of Child Neurology, Maastricht University Medical Center, Maastricht, The Netherlands.
I CuppenDepartment of Child Neurology, Nijmegen University Medical Center, Nijmegen, The Netherlands.
D A SivalDepartment of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, Groningen, The Netherlands.
E H NiksDepartment of Child Neurology, Leiden University Medical Center, Leiden, The Netherlands.
L W Van RhijnDepartment of Orthopedic Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.
M A M Van SteenselDepartment of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
E M J CornipsDepartment of Neurosurgery, Maastricht University Medical Center, Oxfordlaan 10, 6229, EV, Maastricht, The Netherlands.
Maastricht University · NLLeiden University Medical Center · NLRadboud University Nijmegen · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeSprengel's deformity, a rare congenital malformation of the scapula, may be observed in combination with spinal dysraphism. The co-occurrence of these malformations suggests an unknown shared etiology. Therefore, we reviewed the medical records of eight children presenting with both malformations and performed a review of the literature. PATIENTS AND

methodsDatabases from four university medical centers were searched for children presenting between 1992 and 2012 with spinal dysraphism and a Sprengel's deformity.

conclusionThe combination of spinal dysraphism and Sprengel's deformity is rare, and is associated with segmentation defects of the spine and ribs. Although the etiology of both spinal dysraphism and Sprengel's deformity remains unclear, all deformities of the spine, ribs, and shoulder might result from a common genetic defect affecting somitogenesis.

Indexed as

Abnormalities, MultipleChildChild, PreschoolClubfootCongenital AbnormalitiesFemaleHemangiomaHumansInfantInfant, NewbornMagnetic Resonance ImagingMaleMeningomyeloceleNetherlandsScapulaShoulderEmbryologyGeneticsJarcho–Levin syndromeSpina bifidaSpinal dysraphismSpondylocostal dysostosis

Identifiers

PMID23443469
OpenAlexW2169593713

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.