Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Athetosis or dystonia?].

F Turny1, P Jedynak, Y Agid

  • 1Centre d'Investigation Clinique, Fédération de neurologie et INSERM U 289, Hôpital de la Salpêtrière, Paris.

Revue Neurologique
|September 30, 2004
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Clinical characteristics and topography of lesions in movement disorders due to thalamic lesions.

Neurology·2001
Same author

Selected serum cytokines in systemic lupus erythematosus treated with quinagolide.

Lupus·2001
Same author

D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus.

Annals of neurology·2000
Same author

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

Brain : a journal of neurology·2000
Same author

Frequency of the DYT1 mutation in primary torsion dystonia without family history.

Archives of neurology·2000
Same author

Dopaminergic dysfunction in midbrain dystonia: anatomoclinical study using 3-dimensional magnetic resonance imaging and fluorodopa F 18 positron emission tomography.

Archives of neurology·1999
Same journal

Macrophage inclusions in patients undergoing antisense oligonucleotide therapy for ALS or SMA: A retrospective and transversal study.

Revue neurologique·2026
Same journal

Geographic disparities in MRI features of ischemic stroke and small vessel disease: A comparative study between French Guiana and mainland France. Findings from the BECATOUR multicenter registry.

Revue neurologique·2026
Same journal

Continuous subcutaneous perfusion of apomorphine in Parkinson's disease: Towards monotherapy?

Revue neurologique·2026
Same journal

Neuro-Whipple presenting as autoimmune encephalitis.

Revue neurologique·2026
Same journal

Multimodal assessment of minimally conscious state and cognitive motor dissociation in neurocritical care: A critical review.

Revue neurologique·2026
Same journal

Development of a new episodic memory assessment tool (NEM): Preliminary data and clinical perspectives.

Revue neurologique·2026
See all related articles

Athetosis, a distinct neurological condition, is often overlooked but crucial for prognosis. Differentiating it from dystonia is key, as athetosis stems from brain lesions, not heredity.

Area of Science:

  • Neurology
  • Movement Disorders

Context:

  • Athetosis is increasingly subsumed under the broader category of dystonia in Anglo-Saxon literature.
  • Subtle semiological signs, particularly in the hand, can help distinguish athetosis.
  • Early onset suggests a link to early central nervous system development.

Purpose:

  • To re-evaluate the distinct clinical identity of athetosis.
  • To highlight the importance of diagnosing athetosis for prognostic reasons.
  • To differentiate athetosis from hereditary dystonia.

Summary:

  • Athetosis, though rare, presents unique diagnostic features distinct from dystonia.
  • Unlike dystonia, athetosis results from brain lesions and exhibits a stable clinical course.
  • Its early appearance is linked to developmental phases of the central nervous system.

Related Experiment Videos

Impact:

  • Clinical diagnosis of athetosis remains valuable despite its rarity.
  • Understanding athetosis aids in accurate prognosis due to its non-hereditary, lesion-based etiology.
  • Further research is needed to assess treatments like deep brain stimulation for athetosis.