A neurological condition affecting the involuntary movements. It is characterized by brief, non-repetitive irregular muscle contractions. It is seen in patients with Huntington's disease.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
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Data from ClinicalTrials.gov Jan 8, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 8, 2026
Documentation on choreatic disease is limited due to its extreme rarity, affecting fewer than 1 in 1,000,000 people worldwide. This rarity results in fewer systematic clinical studies and less comprehensive data collection, making it challenging to establish a clear genetic or inheritance framework. Additionally, the phenotypic overlap with other movement disorders complicates the characterization of this condition.
The primary clinical features of choreatic disease include gait disturbances and abnormality of movement, both of which are reported in 80-99% of affected individuals. These symptoms can significantly impact daily activities and quality of life, as they may lead to difficulties in coordination and balance.
To navigate your care effectively, seek a neurologist with expertise in movement disorders, particularly those familiar with hereditary ataxias or choreatic conditions. Although there are currently no patient organizations specifically for choreatic disease, you can find support and resources through general rare disease organizations like the National Organization for Rare Disorders (NORD) at rarediseases.org. Additionally, consider reaching out to genetic counseling services, especially if there is a suspicion of hereditary factors. While no registries are currently available, staying informed about emerging research may provide future opportunities.
Actionable guidance for navigating care for choreatic disease
To navigate your care effectively, seek a neurologist with expertise in movement disorders, particularly those familiar with hereditary ataxias or choreatic conditions. Although there are currently no patient organizations specifically for choreatic disease, you can find support and resources through general rare disease organizations like the National Organization for Rare Disorders (NORD) at rarediseases.org. Additionally, consider reaching out to genetic counseling services, especially if there is a suspicion of hereditary factors. While no registries are currently available, staying informed about emerging research may provide future opportunities.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 8, 2026
Consider asking your healthcare providers these condition-specific questions
European rare disease database
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.