DocSym
β
Searchsearch
Search
(G60.2) Neuropathy in association with hereditary ataxia
More details coming soon
127 032 in individuals diagnosis neuropathy in association with hereditary ataxia confirmed
4 684 deaths with diagnosis neuropathy in association with hereditary ataxia
4% mortality rate associated with the disease neuropathy in association with hereditary ataxia
Diagnosis neuropathy in association with hereditary ataxia is diagnosed Men are 3.18% more likely than Women
65 533
Men receive the diagnosis neuropathy in association with hereditary ataxia
2 433 (3.7 %)Died from this diagnosis.
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
0
61 499
Women receive the diagnosis neuropathy in association with hereditary ataxia
2 251 (3.7 %)Died from this diagnosis.
Risk Group for the Disease neuropathy in association with hereditary ataxia - Men and Women aged 10-14
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 95+Less common in women the disease occurs at Age 0-1, 90-94
In Women diagnosis is most often set at age 0-89, 95+
Disease Features neuropathy in association with hereditary ataxia
Absence or low individual and public risk
Neuropathy in association with hereditary ataxia - what does this mean
Neuropathy in association with hereditary ataxia is a condition in which nerve damage occurs due to a genetic mutation in the ataxin-1 gene. this mutation results in an abnormal accumulation of proteins in the neurons, which leads to progressive damage to the nerves and ultimately leads to impaired movement, sensory issues, and other neurological symptoms.
What happens during the disease - neuropathy in association with hereditary ataxia
Neuropathy in association with hereditary ataxia is a neurological disorder caused by a genetic mutation in the ataxin-1 gene, which is responsible for the production of a protein that helps regulate the function of the nervous system. this mutation leads to the accumulation of this protein in the nerve cells, which results in the destruction of the cells and the loss of nerve function, causing symptoms such as numbness, tingling, pain, and weakness in the legs and arms.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete medical history and physical exam
- Blood tests to assess for genetic markers associated with hereditary ataxia
- Neurological exam to assess for muscle weakness, coordination, and reflexes
- Imaging tests such as MRI or CT scans to look for any abnormalities in the brain or spinal cord
- Electromyography (EMG) to measure nerve conduction
- Nerve conduction studies to measure how fast electrical signals travel through nerves
- Nerve biopsy to examine a sample of nerve tissue under a microscope
Treatment and Medical Assistance
Main Goal: To reduce the symptoms of neuropathy in association with hereditary ataxia.
- Engaging in physical therapy to improve muscle strength and coordination
- Taking medications to reduce nerve pain and inflammation
- Using assistive devices such as canes or walkers to improve mobility
- Making lifestyle changes such as quitting smoking and eating a healthy diet
- Practicing relaxation techniques such as yoga or meditation
- Seeking counseling to manage stress and depression
18 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Neuropathy in association with hereditary ataxia - Prevention
The best way to prevent neuropathy in association with hereditary ataxia is to identify those at risk and provide them with regular check-ups and lifestyle advice. this includes avoiding alcohol, smoking, and other activities that may put strain on the body, as well as managing stress levels and maintaining a healthy diet. regular exercise and physical therapy can also help to reduce the risk of developing neuropathy.