Huntington’s disease
Huntington's disease (HD) is a rare and inherited neurological disorder that leads to a progressive breakdown of nerve cells in the brain. It affects movement, cognition, and behavior, causing a wide range of physical and mental symptoms.
HD is caused by a mutation in the HTT gene, leading to the production of abnormal huntingtin protein. This protein builds up in the brain, damaging nerve cells, particularly those in the basal ganglia, which plays a crucial role in movement control.
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Huntington’s disease Conference Speakers
Recommended Sessions
- Bipolar Disorder and Schizophrenia
- Brain Stimulation and Imaging
- Clinical and Translational Neurology
- Front Temporal Dementia
- Molecular Genetics and Neurobiology
- Neurosurgery and Spine
- Alzheimer’s disease
- Alzheimer’s disease and Type 2 Diabetes
- Alzheimer’s disease Diagnosis
- Alzheimer’s disease Imaging
- Amyotrophic lateral sclerosis or ALS
- Animal Models and Translational Medicine
- Ataxia
- Batten Disease
- Behavioral Neuroscience
- Brain Injury
- Brain Pathology and Oncology Research
- Care Practice and Awareness
- Dementia
- Geriatrics and Cognitive Disorder
- Huntington’s disease
- Multiple Sclerosis
- Neurodegenerative Disease
- Neurogenesis
- Neurological disorders
- Neurological Infections
- Neurophysiology
- Neuroscience and Artificial Intelligence
- Ophthalmology and Visual Neuroscience
- Paediatric Neurology
- Parkinson’s disease
- Prion Disease
- Psychiatry
- Space Neuroscience
- Vascular Dementia
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