Parkinson’s disease genetics early-onset cases India Parkin BSN gene mutation treatment - India Today
Parkinson’s disease, traditionally associated with older adults, is increasingly being diagnosed in younger individuals in India. Recent studies highlight that genetics play a major role in these early-onset cases, often appearing in people under 50. Experts warn that early detection is crucial, as symptoms such as tremors, stiffness, and slow movements can be subtle initially. Lifestyle factors, along with hereditary gene mutations, may accelerate the onset. Health professionals stress the importance of genetic testing for at-risk families and early medical intervention to manage progression. With rising awareness, Indian neurologists encourage regular monitoring and prompt treatment to improve quality of life for younger patients. This trend underscores the need for public education on recognizing early signs of Parkinson’s and understanding the genetic predisposition behind it.
The Key points
- Parkinson’s is increasingly seen in younger Indians under 50.
- Genetics are a primary factor in early-onset cases.
- Symptoms include tremors, stiffness, and slow movements.
- Early diagnosis is essential for effective management.
- Gene mutations can accelerate disease progression.
- Family history increases the risk significantly.
- Lifestyle factors may contribute to earlier onset.
- Genetic testing is advised for high-risk individuals.
- Awareness campaigns can help recognize early symptoms.
- Early medical care improves patient quality of life.
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