(G11.2) Late-onset cerebellar ataxia

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149 554 in individuals diagnosis late-onset cerebellar ataxia confirmed

16 151 deaths with diagnosis late-onset cerebellar ataxia

11% mortality rate associated with the disease late-onset cerebellar ataxia

Etiology Pathogenesis Clinical Pattern Diagnostics Treatment Prevention

Diagnosis late-onset cerebellar ataxia is diagnosed Men are 20.27% more likely than Women

89 937

Men receive the diagnosis late-onset cerebellar ataxia

8 312 (9.2 %)

Died from this diagnosis.

100

59 617

Women receive the diagnosis late-onset cerebellar ataxia

7 839 (13.1 %)

Died from this diagnosis.

Risk Group for the Disease late-onset cerebellar ataxia - 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 late-onset cerebellar ataxia

Absence or low individual and public risk

Late-onset cerebellar ataxia - what does this mean

Late-onset cerebellar ataxia is caused by damage to the cerebellum, which is the part of the brain responsible for controlling movement, coordination, and balance. the damage is usually caused by a genetic mutation, but can also be caused by other factors such as stroke, tumor, or infection. symptoms of late-onset cerebellar ataxia include difficulty walking, loss of coordination, and impaired balance.

What happens during the disease - late-onset cerebellar ataxia

Late-onset cerebellar ataxia is a progressive neurological disorder caused by a variety of factors, including genetic mutations, autoimmunity, and environmental factors. the disease is characterized by a loss of coordination and balance due to degeneration of the cerebellum, a part of the brain responsible for coordinating movement. the exact underlying mechanism of the disease is not well understood, but is thought to involve a combination of factors, including genetic mutations, autoimmunity, and environmental factors.

Clinical Pattern

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How does a doctor diagnose

Perform a physical examination to assess coordination, balance, and gait
Order a complete blood count (CBC) to check for anemia or infection
Order a cerebrospinal fluid (CSF) analysis to check for inflammation
Order an electroencephalogram (EEG) to assess the electrical activity of the brain
Order a magnetic resonance imaging (MRI) scan to assess the structure of the brain
Order a computed tomography (CT) scan to assess the structure of the brain
Order genetic testing to identify mutations in genes associated with ataxia
Order an eye examination to assess vision and eye movement
Order a neurological examination to assess coordination, balance, and gait
Order a neuropsychological evaluation to assess cognition

Treatment and Medical Assistance

Main goal of the treatment: To improve the quality of life of the patient and reduce the progression of the disease.

Prescribing medications to reduce symptoms
Physical therapy to improve coordination
Speech therapy to improve communication
Occupational therapy to improve functional activities
Maintaining a healthy diet and exercise regimen
Counseling to help cope with the emotional effects of the disease

24 Days of Hospitalization Required

Average Time for Outpatient Care Not Established

Late-onset cerebellar ataxia - Prevention

To prevent late-onset cerebellar ataxia, it is important to reduce risk factors such as smoking, alcohol consumption, exposure to toxins, and other environmental factors. regular physical activity, a well-balanced diet, and adequate sleep are also important for maintaining good health and reducing the risk of developing this condition.

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