Evidence map›Paper›PMID 26788329›Full record

ArticleJournal of clinical movement disorders2014

The phenomenology and natural history of idiopathic lower cranial dystonia.

Pichet Termsarasab, Donald R Tanenbaum, Steven J Frucht

Abstract read
In one paragraph

Article in Journal of clinical movement disorders, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Pilot Single-Blind Trial of AbobotulinumtoxinA in Oromandibular Dystonia.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Trial
  3. Article
  4. Oromandibular dystonia: from onset to spread a multicenter italian study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Childhood-Onset Spinocerebellar Ataxia 3: Tongue Dystonia as an Early Manifestation.Tremor and other hyperkinetic movements (New York, N.Y.) · 2019
    Article
  10. Pharyngeal Dystonia Mimicking Spasmodic Dysphonia.Journal of voice : official journal of the Voice Foundation · 2018
    Article
  11. Velopharyngeal Dystonia: An Unusual Focal Task-specific Dystonia?Tremor and other hyperkinetic movements (New York, N.Y.) · 2017
    Article
  12. Observational
  13. Medical treatment of dystonia.Journal of clinical movement disorders · 2016
    Review
  14. Oromandibular Dystonia - A Systematic Review.Annals of Indian Academy of Neurology
    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

3 authors.

Pichet TermsarasabDepartment of Neurology, Movement Disorders Division, Icahn School of Medicine at Mount Sinai, 5 East 98th St, first floor, New York, NY 10029 USA.
Donald R TanenbaumDepartment of Neurology, Movement Disorders Division, Icahn School of Medicine at Mount Sinai, 5 East 98th St, first floor, New York, NY 10029 USA.
Steven J FruchtDepartment of Neurology, Movement Disorders Division, Icahn School of Medicine at Mount Sinai, 5 East 98th St, first floor, New York, NY 10029 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany patients with lower cranial dystonia (LCrD) are misdiagnosed, and recognition of this condition by general practitioners and dental health professionals is limited.

methodsWe define the phenomenology and natural history of idiopathic LCrD, presenting in 41 patients with the disorder, the largest series of these patients reported to date.

resultsPhenomenology of dystonia included lower cranial and pharyngeal involvement, jaw opening and jaw closing dystonia, and tongue dystonia. Of 25 newly described patients, 72% (18) were female, average age at onset was 56 years, and delay before correct diagnosis was 3.8 years (0-25 years, median 2 years). Eleven patients (44%) reported a precipitating event, the most common of which was recent dental work. Geste antagonistes were found in 18 patients (72%). Response to treatment was mixed, indicating an unmet therapeutic need.

conclusionsIdiopathic LCrD is often missed and institution of effective therapy is often delayed. The clinical features and natural history of LCrD are similar to other forms of focal dystonia.

Indexed as

Geste antagonisteLower cranial dystoniaOromandibular dystonia

Identifiers

PMID26788329
PMCPMC4676493

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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.