Rare Neurological Diseases
Rare neurological diseases, such as Huntington’s disease, ALS, and Wilson’s disease, present unique challenges due to their low prevalence and complex pathophysiology. These conditions often lack effective treatments, making research into novel therapies and precision medicine crucial. Advances in genetics, biomarkers, and innovative drug development are offering new hope for patients with rare neurological disorders. Collaborative efforts between researchers, clinicians, and patient advocacy groups are accelerating progress in understanding and managing these diseases. Rare neurological diseases are a frontier in neurology, pushing the boundaries of science and medicine to improve patient outcomes.
- Track 23.1-Diagnosis of Rare Disorders
- Track 23.2-Advances in Wilson's Disease
- Track 23.3-Management of Huntington's Disease
- Track 23.4-Challenges in Rare Disease Treatment
- Track 23.5-Role of Genetics in Rare Disorders & Patient Advocacy and Support