Is ataxia cerebellar atrophy?

If the patient has cerebellar atrophy, it will actually cause ataxia. In clinical medicine, if the cerebellum is atrophied, it will not only cause ataxia in the patient, but also cause the patient to have memory loss or cognitive dysfunction. At present, there are many reasons for patients to have brain atrophy lesions, such as family history or inherited genes.

Of course, it cannot be ruled out that it is caused by lesions in the patient's cerebral blood vessels. In addition, some patients have cerebellar atrophy due to cerebral ischemia and hypoxia, or traumatic brain injury.

This is a symptom of cerebellar atrophy.

The cerebellum is responsible for regulating the balance of the human body, and cerebellar atrophy can lead to unsteady walking, which is medically called ataxia. Cerebellar atrophy is a late-onset encephalopathy caused by delayed pathological changes in the innervated area of the original affected nerve due to prolonged ischemia. Whether the disease can be controlled and continues to develop, the analysis of the disease can agree on effective measures, otherwise the disease is prone to delay, more severe neuroatrophy, etc., leading to dementia and paralysis.

**Mainly for the combination of Chinese and Western diseases**and**.

Ataxia may be caused by cerebellar atrophy or excessive mental stress, and ataxia may be caused by excessive life stress, mental stress, and cerebellar atrophy, which may be caused by genetic inheritance. Patients should relax and pay attention to rest, mainly through rehabilitation** to maintain their ability to take care of themselves. There may be slow movements, during this time we must pay more attention to rest, but also to ensure a sufficient sleep do not stay up late, appropriate exercise.

Cerebellar atrophy disease can cause ataxia, the main symptoms of cerebellar atrophy will appear ataxia, memory loss, cognitive dysfunction, cerebellar atrophy disease causes many reasons, some patients are hereditary due to family history, some patients are caused by cerebrovascular disease, and some patients are cerebellar atrophy caused by cerebral ischemia and hypoxia.

There is also a patient caused by traumatic brain injury, it is best to go to a regular hospital for a detailed examination, after clearing, targeted prevention and, cerebellar atrophy disease can not be completely abandoned, can only be targeted prevention, patients must do more outdoor physical exercise in their daily life, eat less greasy food, eat less too salty food, no smoking and alcohol, avoid cold, infection and cold, which can prevent the aggravation of cerebellar atrophy disease.

No. The completion of any action of the body depends on the coordinated movement of a certain group of muscle groups, which is called mutual aid. This coordination mainly relies on the function of the cerebellum to coordinate muscle activity, maintain balance, and help control posture, and also requires the normal muscle strength of the cavity motor system, the balance function of the vestibular nervous system, the coordination of eyes, head, and body movements, and the sensory system's sense of position.

Ataxia can occur with any loss or blight in these areas.

To put it simply, there is an uncoordinated movement of the limbs, such as: 1. Finger-nose experiment Ask the patient to lie on his back and touch the index finger of the examiner in front of him, and then point to the tip of his nose with his index finger, from slow to fast, first open the eyes and then close the eyes, and repeat. Ipsilateral fingering is inaccurate in cerebellar hemisphere lesions, such as accurate fingering when the eyes are opened, and disturbance when the eyes are closed, sensory ataxia.

2. Heel-knee-shin experiment The patient is asked to lie on his back, lift one lower limb up, place the heel on the lower end of the knee of the other lower limb, and then move down along the anterior edge of the tibia, first open the eyes, and then close the eyes and repeat. Movement is unsteady when the cerebellum is damaged, and it is difficult to find the knee with the heel closed in patients with sensory ataxia closed. 3. Other A rapid rotation action:

Ask the patient to straighten the palm of the hand and make rapid pronation and supination movements of the forearm, or use the palm of the hand and the back of the hand to continuously and alternately pat the opposite palm of the hand. b. Difficulty in standing with eyes closed: ask the patient to stand with his heels together, close his eyes, and stretch his hands forward. If you are able to stand firmly when you open your eyes but you can't stand when you close your eyes, you have sensory ataxia.

The clinical manifestations of cerebellar atrophy are as follows:

1. Daily behaviors are manifested as slow autonomous life, cerebellar gait, unsteady standing, wide stride, poor speech, dysphagia, dysarthria, difficulty walking in a straight line, nystagmus, inaccurate vision, and inability to finger and nose, which means that the nose cannot be accurately pointed out when the eyes are closed.

2. Inconvenience in life, manifested as difficulty in defecation, decreased or disordered sexual function, and difficulty in perspiration.

3. Spontaneous sensation, manifested as dizziness, syncope, palpitations.

4. In clinical examination, hypotonia, rapid rotation test, difficulty in standing with eyes closed, heel knee and shin test, finger and nose test all showed positive signs.

5. Imaging examination, CT examination showed that the cerebellum texture was coarse and heavy, the volume was reduced, the superior cerebellar sulcus was wide, the fourth ventricle was enlarged, and the cerebellar vermis was atrophied.

Cerebellar atrophy is mild without any clinical signs and symptoms, and is usually only detected by cranial CT or MRI. In severe cases, dizziness, balance disorders, ataxia, and intention tremor may occur, and some people with weakness and confusion may also have explosive speech. Cerebellar atrophy is precisely a neuroimaging finding that is common in certain genetic disorders and neurodegenerative disorders.

For patients with cerebellar atrophy, common symptoms include ataxia, language dysfunction, eye movement disorders, muscle dysfunction, etc.

1. Ataxia: decreased body coordination, symptoms such as unsteady standing, swaying walking, slightly stretched legs or scissor steps, and at the same time, unable to maintain balance, and irregular writing;

2. Language dysfunction: mainly due to the symptoms of ataxia of the lips, tongue, throat and other muscles, generally manifested as poetry-like speech, slurred speech, slow speech, pronunciation collision, etc.;

3. Ocular motility disorder: mainly eye muscle motility disorder, which will cause the left and right swing of the eyeball;

4. Muscle dysfunction: mainly due to decreased muscle tone, easy to choke when eating or drinking;

5. Others: Some cases are combined with cognitive impairment and movement disorders, such as senile dementia and spinocerebellar differential ataxia.

If the cerebellar atrophy is found by imaging examination, and there are the above symptoms, it is recommended to go to the neurology department in time to see a doctor, use drugs to treat the symptoms, and if the symptoms are severe, you need to cooperate with the training. In addition, it is necessary to quit smoking and alcohol, develop good eating habits, and avoid using drugs that are harmful to brain tissue to avoid aggravating symptoms.

Symptomatic manifestations of cerebellar atrophy ataxia at various stages:

Initial symptoms:

1. Walking is like talking about getting drunk (dizziness).

2. The action response is less flexible, and it is difficult to lift heavy objects.

3. The legs are uncoordinated when going up and down the stairs, the muscles are stiff, and some specific actions cannot be completed accurately, such as running, climbing, playing ball, etc.

4. When standing still, the body will shake back and forth, and it is easy to splash out when carrying water. It is easy to bump into the wall or door frame when walking.

5. There is an obstacle in eye movement, and the target cannot be quickly transferred.

6. Poor ability to distinguish distance, such as playing table tennis without envy.

Cerebellar atrophy is not a disease but a neuroimaging finding. It can be seen not only in some hereditary and degenerative diseases, but also in some acute courses such as the late stage of acute cerebellitis and some drug poisoning, and even in some clinically asymptomatic people, cerebellar atrophy can also be seen in imaging examinations, especially in the elderly. Common features are decreased cerebellar volume and widened sulci on neuroimaging.

It can be divided into localized and generalized cerebellar atrophy. Since the cerebellum is mainly involved in the regulation of somatic balance and muscle tone, patients with cerebellar atrophy often have symptoms such as unstable gait, slurred speech, and ataxia.

Ataxia is one of the symptoms of cerebellar atrophy, which can be accompanied by eye movement disorders, slow eye movements, optic nerve atrophy, retinitis pigmentosa, pyramidal tract signs, extrapyramidal signs, muscle atrophy, peripheral neuropathy and dementia.

The CT finding of hereditary ataxia is cerebellar atrophy. Symptomatic**It can alleviate symptoms: (1) Levodopa can alleviate extrapyramidal symptoms such as rigidity, and toxic stigmine or citicoline (citicoline) can promote acetylcholine synthesis; Baclofen (chloroaniline butyric acid) reduces spasticity, amantadine improves ataxia, and clonazepam is preferred for ataxia with myoclonus; Neurotrophic drugs such as adenosine triphosphate (ATP), coenzyme A, inosinate, and vitamin B group can be tried (2) Surgery**: optic thalamic destruction may be performed (3)**Training physics** and assistive walking equipment may be beneficial.

Cerebellar atrophy disease can cause ataxia, the main symptoms of cerebellar atrophy will appear ataxia, memory loss, cognitive dysfunction, cerebellar atrophy disease causes many reasons, some patients are hereditary due to family history, some patients are caused by cerebrovascular disease, and some patients are cerebellar atrophy caused by cerebral ischemia and hypoxia.

If the patient has cerebellar atrophy, then it can lead to symptoms of ataxia, such as the patient may not hold things steadily, may have an intentional normal walk with a wide step, some patients may even have eating and drinking, in addition, the patient may also experience dizziness, head swelling, etc.

1. Cerebellar atrophy and hereditary neurological ataxia are two different things, but cerebellar atrophy will have symptoms of ataxia, and more precisely, cerebellar atrophy is not a disease, but neuroimaging manifestations. Hereditary ataxia is a disease caused by inherited genes, and cerebellar atrophy are two different things, and the two cannot be equated.

2. Cerebellar atrophy and hereditary ataxia, the two are not the same, so there will be differences in the above, although both have symptoms of ataxia, but at the time, it is necessary to find out the cause of the disease, so it is different in all aspects such as medication and medication, and it is recommended that patients should go to a regular hospital to receive the corresponding **.

3. At the same time as the patient is taking medication, he must carry out the first for cognitive function and mental disorders, you should self-adjust in the psychological aspect, if not, you should find a psychologist to help, you should build a confidence in the disease, as well as self-training, etc., to overcome some negative psychological states.

Hereditary ataxia can also be prevented, that is, to avoid consanguineous marriage, and if the patient carries this gene, elective abortion can be used. Generally speaking, patients with ataxia can get it as long as they pass, train and systematize, and should have confidence in it.

The function of the cerebellum is to regulate muscle tone, maintain balance, and make the function of voluntary activity excellent, and cerebellar lesions can cause ataxia. It is recommended that you go to your local hospital to complete the relevant examinations and make a clear diagnosis.

Cerebellar atrophy disease can cause ataxia, the main symptoms of cerebellar atrophy will appear ataxia, memory loss, cognitive dysfunction, cerebellar atrophy disease causes many reasons, some patients are hereditary due to family history, some patients are caused by cerebrovascular disease, and some patients are cerebellar atrophy caused by cerebral ischemia and hypoxia.

There is also a patient caused by traumatic brain injury, it is best to go to a regular hospital for a detailed examination, after clearing, targeted prevention and, cerebellar atrophy disease can not be completely abandoned, can only be targeted prevention, patients must do more outdoor physical exercise in their daily life, eat less greasy food, eat less too salty food, no smoking and alcohol, avoid cold, infection and cold, which can prevent the aggravation of cerebellar atrophy disease.

Hello! Ataxia refers to the clinical manifestations of disordered coordination, instability and uncoordination of limb movements in the absence of muscle strength. Ataxia can occur with deep sensory, vestibular system, cerebellum, and brain lesions, and is called sensory, vestibular, cerebellar, and cerebral ataxia, respectively.

Cerebellar atrophy is one of the causes! Clinically, cerebellar atrophy can cause attack disorders, and the main symptoms of considerable atrophy will show some memory loss, and some cognitive dysfunction will occur. However, there are many reasons for cerebellar atrophy, such as familial heredity, some patients are caused by cardiovascular and cerebrovascular diseases, and there is another kind of patients caused by cerebral ischemia and hypoxia.

The CT finding of hereditary ataxia is cerebellar atrophy. Symptomatic**It can alleviate symptoms: (1) Levodopa can alleviate extrapyramidal symptoms such as rigidity, and toxic stigmine or citicoline (citicoline) can promote acetylcholine synthesis; Baclofen (chloroaniline butyric acid) reduces spasticity, amantadine improves ataxia, and clonazepam is preferred for ataxia with myoclonus; Neurotrophic drugs such as adenosine triphosphate (ATP), coenzyme A, inosinate, and vitamin B group can be tried (2) Surgery**: optic thalamic destruction may be performed (3)**Training physics** and assistive walking equipment may be beneficial.