Is cerebellar ataxia really inherited?

Ataxia does not have to be genetic.

It can be caused by traumatic brain injury, intracranial hemorrhage, and more.

Genetic ataxia is usually symptomatic as a child.

More than 60 should not be hereditary. It will not be passed on to future generations.

Spinocerebellar ataxia (SCA) is a group of neurological genetic disorders caused by genetic mutations leading to degeneration of the cerebellum, brainstem, and spinal cord. The main clinical manifestations are progressive motor coordination dysfunction and balance disorders. Most are autosomal dominant, but can also be autosomal recessive, X-linked, and mitochondrial inherited.

**Principle. At present, there is no specific method for this disease, and symptomatic treatment can alleviate symptoms. Modalities include medications, surgery, and exercise.

Drugs**. 1. The combined application of buspirone, amantadine and gabapentin can improve the symptoms of ataxia.

2. Levodopa or dopamine agonists can alleviate extrapyramidal symptoms such as rigidity.

3. Neurotrophic drugs such as ATP, coenzyme A, inosine and B vitamins can be tried.

Related medicines. Spirone, amantadine, gabapentin, levodopa, ATP, coenzyme A, inosine, B vitamins.

Surgery**. If the condition requires, optic thalamic dissection may be done.

Other**. Training, physical, and assisted walking may help patients improve their quality of life.

**Cycle. The first cycle of spinal cord and cerebellar ataxia is generally 1 to 3 years, but there may be individual differences due to factors such as the severity of the disease, the first plan, the timing of the file, and the individual's physique.

Cerebellar ataxia is inherited and runs in families, and as long as one person in the family suffers from the disease, there is a 50% chance that the child will inherit it.

Hereditary cerebellar ataxia (neurology) is the most common of all reported ataxias. The pathogenesis is unknown, and the lesions mainly involve the cerebellum, but the spinal cord and cranial nerves can also be partially affected. The mode of inheritance is autosomal dominant, and there is no significant difference in incidence between men and women.

If you find signs of disease, you should go to the hospital for examination in time, and if you find the symptoms, you will be treated in time, so that the effect will be greatly improved, and the condition will not be delayed, and you will not suffer too much pain. Cerebellar ataxia is a disease caused by the degeneration of brain tissue dominated by the cerebellum, and there are many cases that lead to cerebellar ataxia, such as ethanol poisoning, vitamin deficiency, metabolic diseases, vascular diseases, tumors and family inheritance, etc., so there is no accurate statement about whether cerebellar ataxia will be inherited.

Cerebellar ataxia is a disease caused by lesions in the cerebellum itself and the nervous structures associated with the cerebellum, which is more complex, and has a certain relationship with family genetic factors, infection, decreased immune function, tumor compression and other lesions in the brain, so will cerebellar ataxia be inherited? Take you to know the disease of hereditary ataxia.

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 belongs to 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 family does not have cerebellar ataxia. 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 will have brain lesions, such as cerebellar infarction, cerebellar hemorrhage, cerebellar tumor or cerebellar inflammation, etc., it is also possible to cause 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 the cause of cerebellar ataxia.

In general, hereditary spinocerebellar ataxia is common in cerebellar ataxia, and sporadic cases are also common, and the number of inherited generations is different in different inheritance methods, mainly including the following forms:

1. Autosomal dominant inheritance: it is the most common inheritance mode, which is mainly manifested in the continuous generations of patients in the family, and there is a 50% genetic probability for the offspring of the patient with a clear diagnosis, that is, when one of the parents is sick, the children have a 50% chance of developing the disease. In general, the autosomal dominant spinocerebellar ataxia subtype is commonly found in some ethnic patients, also known as SCA3 or Machado-Joseph disease, which is about more than half of the autosomal dominant spinocerebellar ataxia alumina.

Other subtypes such as SCA1, SCA2, SCA3, and SCA6 are rare, while SCA8, SCA12, SCA17, and SCA35 are extremely rare.

2. Autosomal recessive inheritance: the main feature is that when one of the parents is sick and the other parent is normal, the child may carry the disease-causing gene, but will not develop the disease;

Hereditary ataxia is a group of genetic degenerative diseases characterized by chronic progressive cerebellar ataxia, which is characterized by ataxia manifestations, genetic history, and spinal cord, brainstem, and cerebellar damage. In addition to cerebellar and conduction fiber involvement, this group of diseases often involves the pyramidal tract, spinal cord, cranial nerve nucleus, pontine nucleus, spinal ganglia, basal nucleus, and autonomic nervous system. Ataxia gait is the first symptom to emerge and gradually increase in embarrassment, and the most cautious eventually leads to bedridden, overlapping clinical symptoms, and is very complex, and the same family can show a high degree of heterogeneity.

Common symptoms: Friedreich ataxia is the most common idiopathic degenerative disease. Chromosomal recessive ataxia is often early and has unique clinical features, such as childhood.

Progressive gait ataxia of the limbs with neurological signs and symptoms such as pyramidal extrapyramidal signs, dysphonia, deep paresthesias, and non-neurological symptoms such as scoliosis, pes cavus, and cardiac impairment.

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 atrophy usually affects walking. Patients with cerebellar atrophy generally have symptoms such as dizziness, dizziness, unsteady walking, uncoordinated limbs, slurred speech, and plosive sounds, and the patient can be diagnosed by cranial magnetic resonance examination. The cerebellum can regulate the posture and balance of the limbs and coordinate the voluntary movements of the cerebellum, so the main symptoms of cerebellar atrophy are uncoordinated limb function and abnormal posture.

Patients should pay attention to rest when they are flat, so as not to cause blood supply to the brain.

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.