How to treat hereditary cerebellar ataxia

Hereditary cerebellar ataxia.

Clinical presentation. 1.Most of them start at the age of 30 to 60 years, and a few develop at the age of adolescence or 70 years of age. There is a family history of autosomal dominant inheritance, often with ataxia gait as the first symptom, unsteady walking, and easy falling. Thereafter, bilateral upper extremity ataxia may gradually develop.

2.Some cases may have dysphagia, aphonia, speech disorders, emotional instability, wisdom decline, etc., as well as diplopia, eye movement disorders, etc.

3.Weakness in both lower extremities, increased muscle tone, hyperreflexia or hyporeflexia, and positive pathological reflexes.

4.There are no cavus feet or cardiac abnormalities.

Diagnostic differentiation. Basis for diagnosis.

1.The age of onset is late, and there is a family history of autosomal dominant inheritance.

2.Progressively worsening ataxia with a drunken gait.

3.There are no cardiac abnormalities or cavus feet, and skeletal x-rays** are usually normal.

4.Other types of ataxia were excluded, cerebral palsy and motor neuron disease, and cancerous cerebellar ataxia were excluded.

Disease**. **Principle.

1.Symptomatic and supportive**.

2.Acupuncture & ****.

Principles of medication. Drugs within the medication framework can only relieve or alleviate symptoms, and nerve growth factor or cell growth peptide intramuscular injection and nutritional drugs can be used to enhance physical fitness and improve body resistance when conditions permit.

Guess you follow. The best of ataxia**.

Cerebellum altogether.

The kidney is the innate foundation, the essence of the essence, and the main bone. Kidney deficiency and bone shaking: It is mostly due to the deficiency of kidney qi in advanced years, kidney and yang deficiency, and weak support, so that the body leans forward or shakes from side to side when standing, and becomes a disease of unsteady walking.

The cerebellum controls the balance of the human body, resulting in unstable walking, dystrophy of muscles, muscles, muscles, muscles, bones, weakness of limbs, unstable standing, and kidney deficiency as the source of the disease.

Cerebellar ataxia can be divided into two types: hereditary and acquired. Hereditary cerebellar ataxia, there is still a lack of effective solutions, and acquired cerebellar ataxia, first of all, we must understand, common infection, inflammation and tumors, vascular factors, metabolic factors, poisoning, immune diseases, etc., such as patients due to heavy alcohol consumption caused by cerebellar ataxia, it is necessary to quit drinking, B vitamins, in order to get better results. If it is caused by a tumor, it needs to be surgically removed to achieve the goal of cerebellar ataxia.

If it is caused by metabolic encephalopathy Wernicke encephalopathy, B vitamins can be supplemented in large doses, such as vitamin B1 supplementation, to get a better ** effect.

People need a lot of muscles to coordinate to complete any random movement, such as stretching out, bending elbows and other seemingly simple actions, which require many muscles to coordinate to complete. The role of the cerebellum is equivalent to a liaison, responsible for the communication between the brain and the cerebral cortex and subcortex, and can be responsible for the coordination of voluntary movements, limb balance and muscle tension. Therefore, when the cerebellum is damaged, muscle coordination will be problematic, and ataxia such as decreased muscle tone, drunken gait, or intention tremor may occur.

Nowadays, imaging is very advanced, and there are cases of unsteady movement, walking with one deviation and one oblique walk, one foot stretched when walking, or not being able to stand normally, or after standing, the eyes are closed and they fall, these conditions are called ataxia. Nowadays, imaging is very advanced, and there are cases of unsteady movement, walking with one deviation and one oblique walk, one foot stretched when walking, or not being able to stand normally, or after standing, the eyes are closed and they fall, these conditions are called ataxia. How can you tell what is the cause of this ataxia?

One of the biggest ataxias** is the cerebellum, because people have a brain and a cerebellum. The brain is responsible for human intelligence, and the cerebellum is responsible for balance. Cerebellar dysfunction will cause ataxia, which will cause this kind of walking crookedly, some like a drunk, some like a lame leg, in this case, it is ataxia.

To go to the hospital in time, when you get to the hospital, you must first do a CT of the brain, or magnetic resonance. Magnetic resonance imaging or CT can easily see the shape of the cerebellum. If there is ischemia or hemorrhage in the cerebellum, or atrophy of the cerebellum, or severe lesions of the cerebellum, ataxia can be caused.

Therefore, this ataxia related to the morphological state of the cerebellum is called cerebellar ataxia. The disease is easily identified by imaging and clinical diagnosis.

Cerebellar ataxia can be inherited and is called hereditary ataxia. There is no specific method, so the focus should be on prevention. Avoid marriages between close relatives, do a good premarital examination, and try not to get married or have children after marriage if you have a family history.

Physical exercise should be strengthened during the course of the disease to prevent premature bed rest and disability, the disease develops slowly, and is often not life-threatening in the early stage.

Cerebellar ataxia is likely to be inherited, belonging to a familial dominant nervous system lesions, lesions are also more complex, and genetic factors, immune dysfunction and infection factors, tumor compression and other conditions are very related, usually we must pay attention to a reasonable diet, pay more attention to rest.

Spinocerebellar ataxia is usually a genetic disorder and is more common than autosomal dominant inheritance. This means that the disease occurs almost from generation to generation, regardless of gender. At present, there are many types of spinocerebellar ataxia that are related to heredity, and there are more than 40 types, and each one is not exactly the same, and it is very complex.

If there are symptoms of cerebellar atrophy ataxia, it is recommended to see a doctor, especially if you have such a patient in your family, you must go to the doctor, it is best to be able to check the genes, find out**, what type of spinocerebellar ataxia you are, whether you will inherit it to your next generation, your future disease progression, how long will you be unable to walk, bedridden, or even life-threatening, these must be examined to be clear.

Cerebellar hereditary ataxia may be inherited from one generation to the next, but it is not absolute, so there is no need to worry too much. At present, there is no specific drug for this disease**, which can be treated by traditional Chinese medicine, with physiotherapy, such as acupuncture, massage, massage, magnetic therapy, moxibustion, etc., and usually adhere to soothing and gentle exercises, such as walking, yoga, tai chi, aerobics, etc., and have a regular life.

Yes. Ataxia is inherited for several generations, depending on the patient's specific situation, and if it is autosomal dominant, it may generally be inherited in the immediate family; If it is an autosomal recessive disorder, in general, the chance of inheritance depends on the patient's specific situation.

In addition, if ataxia is caused by some secondary factors, such as ataxia caused by lesions of the cerebellum or spinal cord due to intracranial infection, these patients are generally not inherited.

Others are due to nutritional disorders, such as ataxia caused by subacute combined degeneration caused by vitamin B1 or B12, which is generally not inherited.

There are also some patients who are alcoholic due to long-term alcohol abuse.

Spinocerebellar ataxia, which is hereditary, is the main type of hereditary ataxia. Common features are middle-aged onset, autosomal dominant inheritance and ataxia, with prevalence ranging from 8 100 000 to 12.1 million. It is more common than in adolescence and middle age, and most of them are autosomal dominant, and very few are autosomal recessive, or X-linked.

The pathological changes are mainly cerebellar, spinal cord and brainstem degeneration. Clinical manifestations, in addition to cerebellar ataxia, may be accompanied by ocular movement disorders, optic nerve atrophy, pyramidal tract signs, extrapyramidal signs, peripheral neuropathy and dementia.

Cerebellar ataxia, which is a family dominant genetic neurological disease, means that as long as one of the parents has this disease, his children will have a 50% chance of inheriting his disease, and will develop hereditary cerebellar ataxia, he is a genetic disease!

The genetic probability of ataxia is very high, and if one of the parents has the disease, there is a 50% chance that the offspring will develop the disease. Therefore, the impact on future generations is from time to time, and it is immeasurable that it can be inherited for several generations. Ataxia is currently a disease that cannot be improved, the patient's mobility will gradually be lost, and physical exercise should be strengthened during the course of the disease to avoid premature bed rest and disability, the disease is slow to develop, and the early stage is often not life-threatening.

Cerebellar atrophy is a neurological disorder that runs in families, and there is a 50% chance that one of the parents will inherit the disease. After the onset of the disease, these patients walk swayingly, like penguins, so they are called the penguin family. Cerebellar atrophy is a chronic, progressive brain disease that mainly damages the spinal cord and cerebellum, and is usually inherited in families.

Due to the different scope and development process of the lesions, there are many types of clinical signs of cerebellar atrophy, and its main symptoms are unsteady walking, poor movement, weakness in gripping, slurred speech, dizziness, heavy head, head swelling, headache, accompanied by diplopia or blurred vision, swallowing, trembling in writing, and urinary and urinary disorders.

Ataxia can be inherited.

Ataxia may cause patients to have uncoordinated body movements, fine motor difficulties such as eating and writing, abnormal pronunciation, nystagmus, dysphagia and other adverse symptoms, which will seriously affect the patient's daily life in the future.

Patients with hereditary cerebellar ataxia should go to the hospital in time to adjust their medication, the impact of this disease on the human body is relatively large, but it is not necessarily and absolutely inherited from generation to generation, so you should not worry too much. Develop a good habit of regular work and rest, adhere to **, and eat lightly.

But there is a genetic possibility that there is a genetic cause. Therefore, it is recommended that if you have similar symptoms, you should carry out ** medical intervention. This effectively avoids heredity.

Cerebellar ataxia is mainly manifested by chronic degenerative diseases of the central nervous system, cerebellar ataxia develops slowly, if there are no serious cardiopulmonary complications, in most cases it will not affect lifespan, of course, a small number of patients may be bedridden or even disabled, most of this disease has a family history, mainly manifested in autosomal recessive or dominant inheritance, cerebellar ataxia As long as one person has this disease, it may continue to be sick in the later stage, but most of the people who suffer from this disease are men, Men are much more likely to develop the disease than women. Cerebellar ataxia usually begins at the age of 30 to 60 years, and a few develop at the age of adolescence or 70 years of age.

According to clinical evidence, cerebellar ataxia can effectively prolong the normal pressure and hypoxia tolerance time of the brain, improve meningeal microcirculation, promote the growth of nerve fibers, capillary regeneration and the restoration of cell function, thereby effectively improving the symptoms of cerebral hypoxia and ischemia.

Through the above introduction, we must have learned about the knowledge of cerebellar ataxia, if there are such patients around, we should persuade the patient to go to the hospital in time for treatment, the onset of this disease is slow, if you see a doctor in time, cooperate with the hospital to do some ****, as well as the ** of traditional Chinese medicine, I believe that under the conditioning of the hospital, it is still possible to improve the symptoms.

Cerebellar ataxia is caused by neurostructural lesions of the cerebellum itself or related to the cerebellum, which is more complex and related to genetic factors, infections, immune dysfunction, tumor compression, etc. There is a certain genetic predisposition to the disease, but it is not necessarily passed on to future generations. Patients should go to a public hospital on the right track to stop the examination and **, stop functional exercise appropriately, and do not smoke and drink.

1. The ** of any kind of disease is diverse, and similarly, there are many factors or diseases that will also lead to cerebellar ataxia under the joint action, and family genetic inheritance is one of them, because cerebellar ataxia will have a certain genetic tendency, if the family population has suffered from cerebellar ataxia, and the probability of offspring suffering from this disease will be higher than the probability of not having cerebellar ataxia in the family. However, it does not mean that all cerebellar ataxia is inherited because of family genes, because everyone's physical condition and living environment are different, so this family genetic inheritance is not 100%.

2. Cerebellar ataxia is ataxia caused by a variety of ** lesions of the cerebellum, if the body is brain lesions, such as cerebellar infarction, cerebellar hemorrhage, cerebellar tumor or cerebellar inflammation, etc., it is also possible to lead to cerebellar ataxia, and if the usual life does not pay attention to the details of life, resulting in a series of poisoning conditions such as drug poisoning, CO, alcohol poisoning, etc., it is also one of the causes of cerebellar ataxia, because of age, The body's resistance is weakened, and aging is also one of the most important causes of ataxia.

Cerebellar ataxia is a disease with family genes, but because there are many factors affecting the disease, it cannot be said that cerebellar ataxia is 100% genetic, it can only be said that it has a genetic tendency.