Evidence map›Paper›PMID 31127340›Full record

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

The supplementary motor area syndrome and the cerebellar mutism syndrome: a pathoanatomical relationship?

Jonathan Grønbæk, Emanuela Molinari, Shivaram Avula, Morten Wibroe, Gorm Oettingen, Marianne Juhler

Abstract readReview
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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. The Cerebellar Mutism Syndrome: Risk Assessment, Prevention and Treatment.Advances and technical standards in neurosurgery · 2023
    Article
  7. 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

6 authors at 6 institutions in 2 countries.

Jonathan GrønbækDepartment of Neurosurgery, The University Hospital Rigshospitalet, Copenhagen, Denmark. jonathan.kjaer.groenbaek@regionh.dk.
Emanuela MolinariDepartment of Neurology, The Queen Elizabeth University Hospital, University of Glasgow, Glasgow, UK.
Shivaram AvulaDepartment of Radiology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
Morten WibroeDepartment of Neurosurgery, The University Hospital Rigshospitalet, Copenhagen, Denmark.
Gorm OettingenDepartment of Neurosurgery, Aarhus University Hospital, Aarhus, Denmark.
Marianne JuhlerDepartment of Neurosurgery, The University Hospital Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-2652-7495
Aarhus University Hospital · DKAlder Hey Children's NHS Foundation Trust · GBCopenhagen University Hospital · DKQueen Elizabeth University Hospital · GBRigshospitalet · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe supplementary motor area (SMA) syndrome affects adults after tumour resection in SMA neighbouring motor cortex. Cerebellar mutism syndrome (CMS) affects children after tumour resection in the posterior fossa. Both syndromes include disturbances in speech and motor function. The causes of the syndromes are unknown; however, surgical damage to the dentato-thalamo-cortical pathway (DTCP) has been associated with CMS. Thus, an anatomical link between the areas associated with the syndromes is possible. We discuss the syndromes and their possible relationship through the DTCP.

methodsWe identified 61 articles (cohort studies, case reports and reviews) in MEDLINE and Embase searching for CMS, SMA syndrome or DTCP or synonyms and reviewed for evidence linking CMS and SMA.

resultsWe found that SMA syndrome and CMS are similar regarding (1) surgical causation; (2) symptoms including speech impairment, disturbance in motor function and facial dysfunction; (3) delayed onset; (4) the courses of the syndromes are transient; and (5) long-term sequelae are seen in both. Relevant differences include age predominance of adults in SMA syndrome versus children in CMS.

conclusionsThe similarities of the two syndromes could be traced back to their mutual connection through the DTCP and their membership to a cerebro-cerebellar circuit. The connectivity network could explain the emotional changes and speech reduction in CMS. The difference in time of post-surgical onset may be related to the anatomical distance between the surgical damage to the cerebellum and the SMA, respectively, and the effector neural loop underpinning symptoms.

Indexed as

Cerebellar DiseasesCerebellar NeoplasmsMotor CortexMutismAdultChildHumansPostoperative ComplicationsSyndromeCerebellar mutism syndromeDentato-thalamo-cortical pathwayPosterior fossaSupplementary motor areaSupplementary motor area syndrome

Identifiers

PMID31127340
OpenAlexW2945107248

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.