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(G11.8) Other hereditary ataxias
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149 554 in individuals diagnosis other hereditary ataxias confirmed
16 151 deaths with diagnosis other hereditary ataxias
11% mortality rate associated with the disease other hereditary ataxias
Diagnosis other hereditary ataxias is diagnosed Men are 20.27% more likely than Women
89 937
Men receive the diagnosis other hereditary ataxias
8 312 (9.2 %)Died from this diagnosis.
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59 617
Women receive the diagnosis other hereditary ataxias
7 839 (13.1 %)Died from this diagnosis.
Risk Group for the Disease other hereditary ataxias - Men aged 45-49 and Women aged 55-59
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 0-1, 95+Less common in women the disease occurs at Age 0-1, 90-95+
In Women diagnosis is most often set at age 0-89
Disease Features other hereditary ataxias
Absence or low individual and public risk
Other hereditary ataxias - what does this mean
Other hereditary ataxias are a group of genetic disorders caused by a mutation in one of several genes, which can lead to the degeneration of the cerebellum and other parts of the brain. this can cause problems with balance, coordination, speech, and other neurological functions.
What happens during the disease - other hereditary ataxias
Other hereditary ataxias are a group of neurological disorders caused by genetic mutations that affect the cerebellum, the part of the brain responsible for controlling movement. these mutations can lead to impaired coordination, difficulty walking, and an inability to perform fine motor tasks. other symptoms associated with these disorders include slurred speech, vision problems, and cognitive impairment.
Clinical Pattern
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How does a doctor diagnose
- Physical exam to assess coordination, balance, and reflexes
- Neurological exam to assess cognitive and motor abilities
- Genetic testing to identify the specific type of ataxia
- Blood tests to check for vitamin deficiencies or genetic markers
- MRI or CT scan of the brain to look for any structural abnormalities
- EEG to measure electrical activity in the brain
- Eye exam to check for eye movement impairments
Treatment and Medical Assistance
Main Goal: To reduce the symptoms and progression of Other Hereditary Ataxias
- Regular physical therapy and exercise
- Occupational therapy to help with daily activities
- Speech therapy to help with communication and swallowing
- Nutritional counseling to ensure adequate nutrition
- Medications to reduce muscle spasms and improve coordination
- Assistive devices to help with mobility and daily activities
- Surgery to correct any deformities or joint problems
- Genetic counseling to understand the risks of passing the condition to future generations
24 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Other hereditary ataxias - Prevention
The best way to prevent other hereditary ataxias is to ensure that family members are regularly screened for the condition and to provide genetic counseling to those at risk. it is also important to maintain a healthy lifestyle, including a balanced diet and regular exercise, to reduce the risk of developing the condition.