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(G11.9) Hereditary ataxia, unspecified
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149 554 in individuals diagnosis hereditary ataxia, unspecified confirmed
16 151 deaths with diagnosis hereditary ataxia, unspecified
11% mortality rate associated with the disease hereditary ataxia, unspecified
Diagnosis hereditary ataxia, unspecified is diagnosed Men are 20.27% more likely than Women
89 937
Men receive the diagnosis hereditary ataxia, unspecified
8 312 (9.2 %)Died from this diagnosis.
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59 617
Women receive the diagnosis hereditary ataxia, unspecified
7 839 (13.1 %)Died from this diagnosis.
Risk Group for the Disease hereditary ataxia, unspecified - 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 hereditary ataxia, unspecified
Absence or low individual and public risk
Hereditary ataxia, unspecified - what does this mean
Hereditary ataxia is an inherited disorder caused by a mutation in one or more genes, which results in progressive damage to the nervous system. it is marked by a lack of coordination and balance, poor coordination of voluntary muscle movements, and difficulty speaking, swallowing, and walking. symptoms can range from mild to severe and can appear at any age.
What happens during the disease - hereditary ataxia, unspecified
Hereditary ataxia, unspecified is caused by an inherited genetic mutation in a gene that is responsible for controlling the production of certain proteins in the brain. this mutation leads to the destruction of nerve cells in the cerebellum and other areas of the brain, resulting in symptoms such as unsteady gait, lack of coordination, and difficulty with speech and swallowing.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Detailed patient history
- Physical examination
- Neurological examination
- MRI of the brain
- Genetic testing
- Blood tests to check for metabolic disorders
- Electroencephalogram (EEG)
- Cerebellar function tests
- Eye movement tests
- Nerve conduction studies
Treatment and Medical Assistance
Main goal of the treatment: To improve the symptoms of Hereditary ataxia, unspecified
- Physical therapy to improve balance, coordination, and strength
- Occupational therapy to help with activities of daily living
- Speech therapy to improve communication abilities
- Counseling to help with emotional and social issues
- Medications to control symptoms
- Assistive devices to help with mobility
- Vestibular rehabilitation to improve balance and coordination
- Nutritional counseling to ensure adequate nutrition
24 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Hereditary ataxia, unspecified - Prevention
Hereditary ataxia, unspecified, is a genetic disorder that cannot be prevented. however, early diagnosis and treatment can help to reduce its effects and improve quality of life. genetic counseling can help individuals and families understand their risk for developing the disorder. additionally, lifestyle modifications such as regular exercise, a nutritious diet, and avoiding smoking and alcohol can help to reduce the risk of developing other medical conditions that may be associated with hereditary ataxia.