Causes of hereditary ataxia

I feel sorry for the child, it's this at such a young age, but fortunately, the child has been eating the recovery recipe drink to recover.

Hereditary ataxia is a group of inherited degenerative diseases of the central nervous system characterized by chronic progressive ataxia. In addition to cerebellar and conduction fiber involvement, this group of diseases often involves the posterior cord of the spinal cord, pyramidal tract, pontine nucleus, basal ganglia, spinal ganglia, and autonomic nervous system. In addition, it may be accompanied by non-neurological clinical manifestations, such as skeletal deformities, endocrine disorders, myocardial hypertrophy, and conduction block.

The mode of inheritance is mainly autosomal dominant, and sporadic cases are not uncommon.

The main cause of hereditary ataxia is genetic factors. Hereditary ataxia refers to a large group of degenerative diseases of the central nervous system caused by genetic factors, with ataxia dyskinesia and dysmia as the main clinical manifestations, accounting for about 10% to 15% of neurogenetic diseases. The mode of inheritance is mainly autosomal dominant inheritance, but also autosomal recessive inheritance and X-linked inheritance, and sporadic cases are not uncommon.

Hereditary ataxia usually occurs at the age of 20 to 40 years, but there are also infants and older people. Although the clinical symptoms are complex, overlapping, highly genetically heterogeneous and difficult to classify, it has three major characteristics: genetic background passed down from generation to generation, clinical manifestations of ataxia, and pathological changes dominated by cerebellar, spinal cord, and brainstem damage. The main cause of hereditary ataxia is autosomal dominant disorders.

The clinical manifestations are gait instability, ataxia, and difficulty walking in both lower limbs at the same time. When the symptoms are obvious, there will also be a widening of the gait base and swaying from side to side when walking. As the disease progresses, there will be disorders of both upper limbs, deliberately curvature tremor, and slurred speech.

Some patients may also experience dizziness, nausea, vomiting, tinnitus, deafness, facial muscle weakness, difficulty swallowing, and choking on water.

Some patients are accompanied by cognitive function and mental disorders, manifested as inattention, impaired memory, decreased executive ability, depression, anxiety, sleep disorders, behavioral disorders, etc.

If this disease occurs, it is recommended to go to the neurology clinic for timely examination and **.

It is a group of inherited disorders characterized by cerebellar ataxia. It is divided into autosomal dominant inheritance and autosomal recessive inheritance, and generally occurs during puberty. The clinical manifestations are dizziness, weakness to walk, unsteady walking, easy falling, clumsiness of hands and feet, unsteady holding, poor fine motor skills, arthria, dysphagia, and choking on water.

**: First, nourish the nerves. Coenzyme Q10, Citicoline.

Second****. Use the best means to improve the patient's functional impairment. For example, daily functional training, exercise**, active exercise, passive exercise.

Third, physics**. Give medium, microwave, etc.**.

Fourth, acupuncture and massage in traditional Chinese medicine also have an improvement effect on patients' functional impairment.

Ataxia refers to a disorder of coordination of movement with normal muscle strength. Disturbance of the amplitude and coordination of voluntary movements of the limbs, and inability to maintain body posture and balance. However, it does not include coordination impairment in mild limb paralysis, voluntary movement deviation due to ophthalmoplegia, difficulty in voluntary movement due to visual impairment, and apraxia due to cerebral lesions.

Ataxia can occur with deep sensory, vestibular system, cerebellum, and brain lesions, known as sensory, vestibular, cerebellar, and cerebral ataxia, respectively, as well as unexplained factors, some with intellectual deficiency or dementia.

Ataxia is not very familiar to many people, but this disease is a relatively common neurological disease at present, and it is also a very harmful disease.

The root cause of ataxia lies in the damage to the nerve cells in the brain due to various reasons, and the nerve conduction in the brain tissue is blocked, and the normal innervation function cannot be completed.

Hereditary ataxia is a degenerative disease of the central nervous system caused by heredity, accounting for about 10 to 15 of neurogenetic disorders. The inheritance pattern is mainly autosomal dominant inheritance and autosomal recessive inheritance.

1. It is a hereditary disease, specifically You Chun, ataxia is an autosomal dominant genetic disease, the occurrence of ataxia and genetic genes have a very great relationship, there is a gene chain called CAG, which has mutated, which leads to the dysbicity of ataxia, which is a very harmful disease.

2. This genetic change will affect the cerebellum, spinal cord and other parts, resulting in symptoms throughout the body. In severe cases, even the loss of meditation sells all functions and becomes a coma, followed by the symptoms of dementia, and the milder ones are difficulty in speech, unsteady walking, difficulty swallowing, and so on.

3. And many people of all ages may have the disease, once they find out that they have this disease, they should accept it as soon as possible**. Although this disease cannot be completely eliminated, it can still be controlled by using appropriate methods. In addition, the existing condition can be improved, and some of the self-care ability can be restored through acquired training.

Ataxia is only a clinical manifestation, and there are many causes of ataxia in patients, and ataxia is not necessarily genetic. Spinocerebellar ataxia is caused by a genetic mutation, so ataxia can also be inherited. Genetically related ataxia, there is currently a lack of effective means of transport, mainly for the training of brain cells, neuroprotective drugs for brain cells.

Cerebellar diseases, such as cerebellar hemorrhage, cerebellar infarction, cerebellar inflammation caused by ataxia, can be acupuncture to carry out the disease**, when the disease is reduced, alleviated, ataxia will also be reduced until remission, so the ataxia caused by these causes is not inherited. It is necessary to analyze the specific condition and find a specialist for a face-to-face consultation. A neurologist will give a detailed physical examination and conduct a search to determine whether it is hereditary ataxia or acquired ataxia, and make a specific decision.

Is malfunction a genetic disorder? Ataxia is not a genetic disorder.

Ten in total, is it a pre-reed hereditary disease? It has both internal and external causes, and there is a hereditary dysfunction of the ability to grasp and argue, that is, the internal cause, and the external cause is caused by the abnormal law of life and life.

You are a broken hereditary, so we should look at it correctly and rationally.