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

[Chorea].

P Vieregge1

  • 1Klinik für Neurologie, Klinikum Lippe, Lemgo. peter.vieregge@klinikum-lippe.de

Therapeutische Umschau. Revue Therapeutique
|January 16, 2007
PubMed
Summary
This summary is machine-generated.

Chorea, characterized by involuntary dance-like movements, is a key symptom of Huntington's disease and other neurological disorders. Effective symptomatic relief is available through targeted medications.

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

The relevance of clinical subtypes for disease course, family history and epidemiological variables in Parkinson's disease.

European journal of neurology·2013
Same author

Autosomal dominant Parkinson's disease in a large German pedigree.

Acta neurologica Scandinavica·2011
Same author

[Hirayama disease in Germany: case reports and review of the literature].

Der Nervenarzt·2011
Same author

[When should we start medical treatment in Parkinson disease].

Fortschritte der Neurologie-Psychiatrie·2010
Same author

German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations.

Parkinsonism & related disorders·2008
Same author

Are neuropsychological tests useful in screening for the genetic risk of Parkinson's disease?

Parkinsonism & related disorders·2008

Area of Science:

  • Neurology
  • Movement Disorders

Background:

  • Chorea is defined by involuntary, irregular, and nonrepetitive muscular contractions, often described as dance-like.
  • Huntington's disease is a primary genetic condition where chorea is a core symptom, presenting with neurological and psychiatric features.
  • Chorea can also manifest in rare neurodegenerative diseases, inborn errors of metabolism, and various acquired conditions in adults.

Purpose of the Study:

  • To provide a comprehensive overview of chorea, its underlying causes, and management strategies.
  • To highlight the differential diagnostic importance of chorea, particularly paroxysmal choreoathetoses.
  • To discuss the symptomatic treatment of chorea in various clinical contexts.

Main Methods:

  • Literature review of chorea and associated conditions.

Related Experiment Videos

  • Analysis of clinical presentations and diagnostic criteria.
  • Summary of therapeutic options for symptomatic relief.

    • Main Results:

    • Chorea presents as a core symptom in Huntington's disease, a rare neurodegenerative disorders, and metabolic conditions.
    • Paroxysmal choreoathetoses require careful differential diagnosis from seizures and transient ischemic attacks.
    • Symptomatic chorea in adults can arise from diverse drug-induced, metabolic, infectious, immunological, toxic, and vascular causes.

    Conclusions:

    • Chorea is a complex motor symptom with diverse etiologies, ranging from genetic disorders to acquired conditions.
    • Accurate diagnosis is crucial for appropriate management, especially differentiating from other neurological events.
    • Pharmacological interventions can effectively manage the involuntary movements associated with chorea, improving patient quality of life.