Familial Parkinson disease type 1
A familial form of Parkinson disease inherited in an autosomal dominant manner due to mutation in the alpha-synuclein gene (SNCA) on chromosome 4q21. Also known as PARK1
Medical disclaimer
The information on this page is for educational and informational purposes only and does not constitute medical advice in any way.
- It does not replace the advice of a physician, pharmacist or other healthcare professional.
- It does not represent a prescription of drugs, diagnostic exams or therapies.
- In case of symptoms, doubts or concerns about your health, always consult a qualified physician.
In case of emergency call 911 (US) or 112 (EU).