Any Parkinson disease in which the cause of the disease is a mutation in the LRRK2 gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
The documentation surrounding autosomal dominant Parkinson disease 8 is limited due to its relatively recent identification and the ongoing efforts to characterize its clinical features. Additionally, because this condition affects a smaller population compared to other forms of Parkinson's disease, systematic clinical studies have been sparse, leading to gaps in our understanding.
To navigate your care effectively, consider seeking a neurologist who specializes in movement disorders, particularly those with experience in genetic forms of Parkinson's disease. While there are currently no patient organizations specifically for autosomal dominant Parkinson disease 8, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information. Additionally, exploring participation in clinical trials may offer access to cutting-edge research and therapies. Genetic counseling could also be beneficial to discuss the implications of the autosomal dominant inheritance pattern for you and your family.
There are currently 6 active clinical trials investigating various aspects of autosomal dominant Parkinson disease 8. These trials may explore potential therapies or interventions aimed at managing symptoms or slowing disease progression. For more information on these trials, you can visit ClinicalTrials.gov and search for 'autosomal dominant Parkinson disease 8'.
Actionable guidance for navigating care for autosomal dominant Parkinson disease 8
To navigate your care effectively, consider seeking a neurologist who specializes in movement disorders, particularly those with experience in genetic forms of Parkinson's disease. While there are currently no patient organizations specifically for autosomal dominant Parkinson disease 8, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information. Additionally, exploring participation in clinical trials may offer access to cutting-edge research and therapies. Genetic counseling could also be beneficial to discuss the implications of the autosomal dominant inheritance pattern for you and your family.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. 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.