Rare and complex brain disorders encompass a wide range of neurological conditions that are often difficult to diagnose and treat due to their uncommon nature and intricate symptoms. These disorders, such as Huntington's disease, amyotrophic lateral sclerosis (ALS), and certain genetic syndromes, can present with a combination of motor, cognitive, and psychological symptoms that vary greatly from patient to patient. Research in this field focuses on identifying the genetic, molecular, and environmental factors that contribute to these conditions, as well as developing targeted therapies. Advances in genetic testing, neuroimaging, and personalized medicine are helping to improve diagnostic accuracy and treatment options for individuals with rare brain disorders. A multidisciplinary approach, involving neurologists, geneticists, and rehabilitation specialists, is essential for providing effective care and support to those affected by these challenging conditions.
Title : Scalp acupuncture with functional electrical stimulation for the treatment children with autism spectrum disorder
Zhenhuan Liu, Guangzhou University of Chinese Medicine, China
Title : Perception and individuality in patient cases identifying the ongoing evolution of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
Ken Ware, NeuroPhysics Therapy, Australia
Title : A structure-based strategy to target pathogenic α-synuclein in Parkinson’s disease
Salvador Ventura, Autonomous University of Barcelona, Spain
Title : Rabies: Challenges in taming the beast
Alan C Jackson, University of Calgary, Canada
Title : Designing and managing intelligent and ethical transformed health and social care ecosystems
Bernd Blobel, University of Regensburg, Germany
Title : Understanding Alzheimer's disease biomarkers across diverse populations - Opportunities and Insights for novel prevision medicine approaches
Sid O Bryant, Texas College of Osteopathic Medicine and University of North Texas Health Science Center Fort Worth, United States