Huntington’s disease
Huntington’s disease is inherited from Parents and often symptoms will be more like Parkinson’s disease which include problem with mood, mental abilities, Swallowing, Speaking, Sleep Disturbances followed by loss of co-ordination and unsteady gait. A gene called HTT (Huntingtin) which is responsible for coding protein Huntingtin, if any mutation to that gene it will cause disturbances in the brain and results in death of brain cell and leads to Huntington’s disease. Abnormalities with the mutant huntingtin include Cardiac Failure, Weight Loss, Osteoporosis, reduced glucose level. This condition is normally observed in the individuals under the age of fifties.
- Neuronal Replacement
- Transcriptional Dysregulation
- Cognitive Behavioural Therapy
Related Conference of Huntington’s disease
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Huntington’s disease Conference Speakers
Recommended Sessions
- Clinical Trials in Parkinson’s diseases
- Diagnosis for Parkinson’s disease
- Epidemiology of Parkinson’s
- Free Radicles and Aging in Parkinson’s
- Huntington’s disease
- Insights and therapeutics: Parkinson’s disease
- Mitochondrial Dysfunction
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- Parkinson Disease
- Parkinson’s disease: Complications
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