How to see brain atrophy and how to identify brain atrophy

1.Systemic symptoms In the early stage of the lesion, patients often have dizziness and headache, insomnia and dreams, soreness in the waist and knees, numbness in the hands and feet, tinnitus and deafness, and gradually become unresponsive, slow in movement, muttering, and answering questions that are not answered. In the physical aspect, it is often manifested as senile state of the dragon, white teeth, dryness, pigmentation, or hemiplegia, epilepsy, ataxia, tremor, etc., and neurological symptoms may or may not be present.

2.Memory impairment Memory impairment occurs early, such as frequent loss of objects and forgetting promised things. As the disease progresses, it gradually leads to complete loss of memory.

3.Changes in Personality and Behavior Personality changes are often an early symptom of the disease, in which the patient becomes depressed and dislikes to interact with others; or manifested as a lack of ideals, desires, and feelings for children and relatives; or have rigid and bizarre living habits, impatient personality, increased speech or verbosity, suspicious and selfish; or have a special concern for their own health and safety, often entangled by some minor discomfort; or amnesia or mania, with delusions, visual hallucinations, auditory hallucinations, aphasia, and agnosia. All high-level emotional activities, shame, responsibility, honor, and morality are reduced to varying degrees, and sleep rhythm changes may also occur.

4.Mental retardation and dementia are manifested as a general decline in intellectual activities such as comprehension, judgment, and numeracy, which makes it difficult to adapt to social life and be incompetent for work and household chores; Gradually, I can't correct my name, age, I don't know how to eat and I don't know how to get hungry, I don't know how to return after going out, and I collect waste paper and miscellaneous items as treasures. In the later stage of the disease, he was bedridden all day long, unable to take care of himself, did not care for himself, incontinent and urinary, slurred speech, slurred speech, and finally complete dementia.

Can brain atrophy be seen well? Can the sequelae of nasopharyngeal carcinoma and brain atrophy be seen well?

Sequelae of radiotherapy for nasopharyngeal carcinoma. For patients with early-to-mid-stage dementia, current medication can control disease progression. I don't know if I've been examined in the neurology department of my local hospital, and what type of dementia it is? This is a good way to recommend medication.

Diagnostic examination of cerebral atrophy: early manifestations are headache, dizziness, gradual loss of memory, decreased or even loss of judgment of time, place, and orientation (such as not being able to find a home after going out), fragmented thinking, major things are ignored, and small things are entangled, mental retardation is reduced, mental malaise, apathy, slow response, lazy speech, slow movement, indifference to surrounding affairs. Personality changes are manifested as selfishness, subjectivity, paranoia, anxiety, suspiciousness, irritability, and incoherence.

Patients may have forgetfulness or mania, even indecent activities, unsteady movement, trembling hands and feet, staggering, inability to walk in a straight line, incontinence, and decreased or lost sexual function. And there are delusions, visual hallucinations, auditory hallucinations, aphasia, agnosia, and then become senile vascular dementia.

Your situation needs to do a cerebral blood flow map, brain MRI brain CT brain color ultrasound suggests that you should go to the hospital ZWA to check the situation in detail, timely conditioning is better, don't worry too much, go to the hospital to infusion blood activation and stasis drugs**, I wish you soon**.

Dementia, mental retardation, personality changes, memory and behavioural impairments are symptoms of brain atrophy.

In order for the brain to function and think normally, and to prevent the invasion of brain viruses, the elderly must insist on supplementing the brain with the nutrients they need for a long time. As a pure natural active ingredient extracted from precious tree species, maple glycoside can not only prevent brain cell aging and make people live longer, but also improve cerebral blood circulation, ensure the adequate supply of blood oxygen to brain cells, promote metabolism, prevent and improve brain diseases well, and also help the recovery of sequelae in sick people.

The symptoms of cerebral atrophy are unresponsiveness and slurred speech, which is similar to but different from Alzheimer's disease.

Brain atrophy begins to decline memory.

In the early stage, it manifests as headache, dizziness, gradual memory loss, decreased or even loss of judgment of time, place, and orientation (such as not being able to find a home after leaving home), and fragmented thinking.

Deficiency of qi and blood, cerebrospinal insufficiency and cause this disease, so when the cerebellar atrophy** should be based on replenishing qi and nourishing blood, nourishing the brain and strengthening the brain. Commonly used traditional Chinese medicines: purple river car, longan meat, Yizhiren, sour jujube kernel, ginseng, atractylodes, poria cocos, angelica, white peony, yam, polygonatum essence, astragalus, etc., can be added or subtracted with symptoms.

Cerebellar atrophy is a chronic, progressive disease with mild early symptoms that can be difficult to detect. Here are some common symptoms of cerebellar atrophy:1

Balance and coordination disorders: One of the most common symptoms of cerebellar atrophy is balance and coordination disorders. Patients may feel unsteady, shaky, or wobbly, especially when walking, standing, or turning.

2.Muscle stiffness: Cerebellar atrophy can also cause muscle stiffness and uncoordinated movements, manifested by muscle rigidity, tremors, or twitching.

3.Nystagmus: Cerebellar atrophy can also be associated with nystagmus, which can blur the patient's vision and affect their balance and coordination.

4.Intellectual and cognitive impairment: As cerebellar atrophy progresses, the patient's intelligence and cognitive abilities may also be affected.

They may become confused, have amnesia, have difficulty concentrating, and become obsessed with complex tasks. If you suspect that you or a family member may have cerebellar atrophy, it is advisable to see your doctor as soon as possible. Doctors usually perform physical examinations, neurological examinations, imaging tests (such as MRI and CT scans), etc., to confirm the diagnosis of cerebellar atrophy. 【

The occurrence of cerebellar atrophy can be determined by routine blood examination, cranial CT examination, magnetic resonance imaging examination, etc., and timely medical attention is required**.

1. Routine blood examination.

If the inside of the brain is infected by bacteria or viruses, and it is not timely and effective, it will also induce cerebellar atrophy, which can be determined by routine blood examination, and the infection can also be ruled out to a certain extent.

2. Cranial CT examination.

It is mainly used to detect whether there is an abnormality in the central nervous system, and can be used to detect cerebral atrophy, hydrocephalus, leukoencephalopathy, intracranial tumors and other diseases. If cerebellar atrophy is present, the diagnosis can be confirmed by cranial CT examination.

3. Magnetic resonance imaging examination of the reeds.

Magnetic resonance imaging mainly uses the hydrogenous macromask nucleus in tissue cells to resonate under the action of magnetic field, which can be used to check for intracranial tumors, cerebral infarction, cerebral hemorrhage and other diseases. If there is a cerebral infarction, cerebellar atrophy can also be caused, and the diagnosis can be confirmed by this test.

In addition to the above common examination methods, there are other examination methods, such as rapid rotation test examination, rebound test examination, liver and kidney function test, etc. After diagnosis, the patient should be treated in time to avoid delaying the condition. Patients can follow the doctor's instructions with drugs such as clonazepam tablets and buspirone hydrochloride tablets**, and can also be assisted by **training and other methods**.

Cerebellar atrophy is a more serious neurological disease, the harm to the body is very great, but also more worrying and frightening, cerebellar atrophy is actually a family dominant inherited nervous system disease, as long as one of the parents is a patient with this disease, the probability of inheritance of children will be relatively large, and the complications caused are also very many, which may lead to inconvenience in walking, physical weakness, and affect normal work and life.

Cerebellar atrophy symptoms manifest differently in different parts of the body, as follows:

1. Eyes: mainly nystagmus, if it is a large nystagmus, blurred vision may occur;

2. Throat: unclear speech or speaking like drunkenness, with blast-like pronunciation and not fluent, swallowing dysfunction will cause choking on drinking water, choking on drinking water, and obvious choking when eating;

3. Limbs and torso: uncoordinated fine hand movements, such as crooked handwriting, uncoordinated movements such as sewing needles and dressing.

The legs show unsteadiness in walking, a drunken gait, and inability to walk in a straight line. There is also unsteady trunk ataxia, swaying from side to side when getting up, and slowly getting up to sit up.

Cerebellar atrophy**.

At the current level of medicine, there is still a lack of effective methods for the cerebellar atrophy that has been formed. Therefore, it is mainly for the intervention of some controllable amino gens, and on this basis, some drugs that can improve the patient's ataxia can be selected to partially improve the patient's clinical symptoms. Neural stem cell transplantation is one of the research directions of cerebellar atrophy in the future, but it is currently limited by ethics and the technical level is not mature, so it is rarely used in clinical practice.

Spinocerebellar atrophy is what we often call cerebellar atrophy. The disease runs in families. This disease is a neurological disease.

If only one parent is likely to have the disease, the probability of the child having the disease is as high as 50 percent. When the patient has this disease, he will feel wobbly when he walks, just like a penguin, so some people call this disease penguin disease. Traditional Chinese medicine believes that the occurrence of cerebellar atrophy is often closely related to kidney deficiency, and classifies this disease as a syndrome of impotence.

Step Method:

1. Cerebellar atrophy can be judged by self-examination in addition to regular hospital examinations. For example, when the patient is standing on his own and his feet are closed, his eyes are closed, and if he or she finds that he or she feels unsteady when standing, he should suspect that he or she has cerebellar atrophy.

2 Of course, cerebellar atrophy can be diagnosed with cerebellar atrophy in addition to self-examination. For example, an MRI scan of the brain can clearly observe the cerebellum to see if atrophy has occurred. In addition, DNA analysis can also detect cerebellar atrophy that runs in families.

3 Cerebellar atrophy tends to run in families and is chromosomal recessive. Patients who develop the disease around the age of 20 may be chromosomally dominant. The occurrence of this disease is caused at the genetic level by a problem with the gene fragment between 9q13 and q21.

This genetic problem can cause ataxia defects.

Precautions. There is also a simple self-examination method for cerebellar atrophy, that is, when the patient stands on one foot and closes his eyes at the same time, if he feels that it is difficult to maintain his or her standing, or if there is no way to stand on one foot at all, there may be cerebellar atrophy.

With cerebellar atrophy, most of them mean that it is inconvenient to walk, and the hands and feet are not dexterous or numb.