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(F02.2*) Dementia in huntington disease
More details coming soon
NaN% mortality rate associated with the disease dementia in huntington disease
Diagnosis dementia in huntington disease is diagnosed Prevalent in Women Only
0
Men receive the diagnosis dementia in huntington disease
0 (No mortality)Died from this diagnosis.
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Women receive the diagnosis dementia in huntington disease
0 (No mortality)Died from this diagnosis.
Risk Group for the Disease dementia in huntington disease - Men and Women aged 0
No Cases of the Disease Dementia in Huntington disease identified in Men
Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 0-95+
No Cases of the Disease Dementia in Huntington disease identified in Men
Disease Features dementia in huntington disease
Absence or low individual and public risk
Dementia in huntington disease - what does this mean
Huntington disease is a progressive neurological disorder caused by a genetic mutation that results in the gradual death of cells in certain parts of the brain. this leads to a decline in cognitive ability, including memory, language, problem solving, and executive functioning, resulting in dementia.
What happens during the disease - dementia in huntington disease
Huntington disease is an inherited neurological disorder caused by a mutation in the huntingtin gene. this mutation leads to the production of an abnormal, toxic protein that accumulates in the brain, causing progressive damage to the cells that control movement, cognition, and behavior. this damage leads to the symptoms of dementia, including memory loss, confusion, and difficulty with language and decision making.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Review of medical history
- Physical examination
- Neurological examination
- Cognitive testing
- Brain imaging (CT or MRI scan)
- Genetic testing
- Psychiatric evaluation
- Psychosocial assessment
- Laboratory tests
Treatment and Medical Assistance
Main goal of the treatment: To reduce the symptoms of dementia in Huntington disease.
- Medication to reduce aggression and irritability
- Physical therapy to maintain muscle strength and coordination
- Occupational therapy to help with daily activities and tasks
- Speech therapy to maintain communication skills
- Counseling to help with emotional well-being
- Nutritional counseling to maintain a healthy diet
- Social activities to maintain social connections
- Cognitive stimulation activities to maintain cognitive function
No Hospitalization Required
Average Time for Outpatient Care Not Established
Dementia in huntington disease - Prevention
The prevention of dementia in huntington disease is based on early diagnosis and treatment of the disease. this includes regular monitoring of symptoms, timely management of medical and psychiatric issues, and lifestyle modifications such as physical activity, healthy eating, and cognitive stimulation. additionally, medications such as antipsychotics, anticonvulsants, and mood stabilizers may be used to help manage symptoms and prevent or delay the onset of dementia.