Is muscle atrophy in the extremities necessarily due to motor neuron disease?

Updated on healthy 2024-06-24
13 answers
  1. Anonymous users2024-02-12

    Motor neuron disease is a relatively common disease, and many athletes will develop this disease, mainly due to long-term high-intensity exercise, which can lead to motor nerve injury, which can lead to the development of the disease. The onset of motor neuron disease is accompanied by significant symptoms of muscle atrophy and muscle weakness, which require adequate attention.

    Motor neuron disease is no stranger to everyone, and many people in their lives are susceptible to this disease. The initial stages of MND can lead to certain physical injuries that may cause pain and numbness that most people do not pay enough attention to. When the disease progresses severely, it can lead to muscle wasting and muscle weakness.

    So is muscle wasting a motor neuron disease? Next, we will introduce the symptoms and manifestations of motor neuron disease.

    If you have muscle wasting, you may be suffering from MND, so you can't ignore it. If it is not controlled in time, it is likely to lead to limited movement in the body. Therefore, it is necessary to take an active ** at the onset of the disease.

    Choose the appropriate method to do it** and be able to return to a healthy body as soon as possible. Motor neuron disease is extremely harmful to people's physical and mental health, and it is necessary to insist on early detection and early detection to get rid of the disease as soon as possible. After muscle wasting, it is advisable to eat more protein-rich foods.

    Symptomatic manifestations of motor neuron disease.

    1. Muscle weakness.

    After MND, the most obvious symptom is muscle weakness. At this time, there will be obvious symptoms of muscle weakness, and it is necessary to adhere to the timely **, and you can carry out appropriate exercise. Don't become lazy at the same time as your muscles are weak, as this will only make the symptoms of the disease worse.

    2. Muscle atrophy.

    Muscle atrophy is a specific manifestation of the severe development of motor neuron disease, and with the severity of the disease, the physical discomfort will become more and more obvious, and the initial stage is only muscle weakness. Due to the lack of active exercise, it will lead to the slow atrophy of muscles, which will cause certain obstacles to people's normal exercise. Therefore, it is necessary to take it in a timely manner, and at the same time make positive adjustments from the diet.

    Motor neuron disease is a relatively harmful disease, can not ignore this disease, need to choose the early stage of the disease, the appropriate **, in order to make the symptoms of the disease can be reasonably controlled. After the development of motor neuron disease, it will cause two obvious symptoms on the patient's body, namely muscle weakness and muscle atrophy. Adhere to the timely **, you can return to a healthy physical state as soon as possible.

  2. Anonymous users2024-02-11

    Motor neuron disease often causes muscle wasting.

    Motor neuron disease (MND) is a series of chronic progressive and neurodegenerative diseases characterized by a series of upper and lower motor neuron damages. The clinical presentation is a different combination of upper and lower motor neuron lesions, characterized by muscle weakness and muscle atrophy, which may be accompanied by bulbar palsy and pyramidal tract signs.

    At present, the pathogenesis is not fully understood, and there are many hypotheses, including genetic mechanisms, oxidative stress, excitotoxicity, neurotrophic factor disorders, autoimmune mechanisms, viral infections, and environmental factors.

    At present, there is no best way for motor neuron disease, mainly to improve clinical symptoms and prevent complications, and the commonly used drug is riluzole.

  3. Anonymous users2024-02-10

    Is muscle atrophy a motor neuron condition? He's not, of course not? He is not a motor neuron disease with muscle atrophy.

  4. Anonymous users2024-02-09

    Muscle atrophy, weakness, and impaired movement may occur.

    Regardless of whether the condition of motor neuron patients is weak spleen deficiency, spleen and kidney yin deficiency, spleen and kidney yang deficiency, liver and blood deficiency, qi and blood deficiency, heart and blood deficiency, lung deficiency and phlegm dampness, etc., they should eat less cold and more warm food. For example, mustard greens, mung beans, kelp, seaweed, zepam, cabbage, daylily, watermelon, bitter gourd, winter melon, etc. are all cold foods and should be avoided as much as possible.

    Generally, patients should eat more sweet and warm tonic foods, such as: millet, jujube, hawthorn, yam, angelica, red adzuki bean, lotus seeds, raisins, walnut kernels, ginger, beef, mutton, black chicken, etc., and you can also buy a bottle of pure natural royal jelly, which is most conducive to enhancing self-immunity and helping the recovery of motor neuron disease. Sweet food can play a role in nourishing, neutralizing, and alleviating urgency, so it is nourishing and strong, regulating the five internal organs, qi, blood, yin, and yang of the human body.

    The disadvantages of motor neuron disease are unknown to this day, and the disease is slowly progressively worsening after the onset of the disease, but nerve growth factor or cell growth peptide intramuscular injection can be used**, and there is no specific measure to stop the progression of the disease. However, if you can take care of it carefully and strengthen the comprehensive support of symptoms**, you can greatly alleviate symptoms and prolong life. Patients and their relatives are advised to go to a qualified neurological disease specialist for diagnosis and treatment due to the strong specialization in the diagnosis and treatment of motor neuron disease, and not to trust social travel doctors to avoid misdiagnosis and treatment.

  5. Anonymous users2024-02-08

    Diseases can lead to muscle atrophy, impaired or loss of motor function. For the disease of the athletic god type local meridian yuan, there is no effective way to ,.. the deficiency of **

  6. Anonymous users2024-02-07

    MND does cause muscle wasting, but if a patient has muscle wasting, it is not always MND. In general, MND belongs to a group of unclear, selective, chronic progressive neurodegenerative diseases of the spinal cord, brainstem motor nerves, metacortex, pyramidal cells, and pyramidal tracts.

  7. Anonymous users2024-02-06

    If the patient has motor neuron disease, these patients are prone to symptoms such as muscle atrophy and weakness. For these patients, a combination of multiple methods is often required, including acupuncture, symptomatic therapy, and exercise.

    Such patients tend to be very long and costly. If it is not timely**, the patient may experience respiratory failure, dyspnea, etc. These patients require ventilators to assist ventilation if necessary, as well as endotracheal intubation.

    If there is dysphagia and choking on water, a nasogastric tube diet is required to ensure the nutrition and energy of the patient's diet.

  8. Anonymous users2024-02-05

    Muscle atrophy occurs in MND, which can be chosen, oral vitamin E and vitamin B, or immunosuppressants can be selected for early progress** and prevention, and at the same time, you should choose, pay more attention to rest, and use neuroregenerative drugs**.

  9. Anonymous users2024-02-04

    You can try Chinese medicine, what are the symptoms now.

  10. Anonymous users2024-02-03

    Although MND presents with clinical symptoms of muscle wasting, not all muscle wasting is MND and may be caused by other diseases; It may even be direct atrophy, i.e., direct muscle atrophy, which may not be associated with MND.

    Motor neuron disease (MND) is a group of chronic, progressive neurodegenerative diseases of the anterior horn cells of the spinal cord, motor neurons of the brainstem, pyramidal cells of the cortex, and pyramidal tract of the spinal cord by unknown choice.

    Most people die within three to five years of onset of symptoms, so the prevalence of the disease is close to the incidence rate.

    The diagnosis of motor neuron disease needs to be confirmed by detection of spinal cord, spinal fluid and electromyography, and it is recommended to go to the internal medicine department in time after muscle atrophy to confirm the diagnosis of symptoms**.

  11. Anonymous users2024-02-02

    Neuronal muscular dystrophy should refer to motor neuron disease, motor neuron disease is a degenerative disease of unknown causes of upper and lower motor neurons, what causes it is not clear, and it is not clear now, so there is no best way to this disease, there is no good way, for example, it can occur in upper motor neurons, and it can also occur in lower motor neurons, which are roughly four diseases.

    Primary lateral sclerosis, which occurs in the upper motor neurons, occurs in the lower motor neurons, progressive spinal muscle atrophy, and the upper and lower neurons are damaged, and the disease occurs in the brainstem, progressive saline paralysis. If it occurs in the anterior horn cells of the spinal cord, called amyotrophic lateral sclerosis, you may be referring to neurogenic muscular dystrophy as amyotrophic lateral sclerosis. At present, there is a drug called riluzole, also called lirutai, which can delay the progression of this disease for a certain period of several months, but it cannot fundamentally solve any problems, so after diagnosing this disease, it is mainly symptomatic treatment, if there is dyspnea, use a ventilator as soon as possible to maintain the patient's breathing and ensure the patient's life safety.

  12. Anonymous users2024-02-01

    Neuromuscular atrophy is not a single disease, it is a general term for diseases that cause muscle atrophy due to neuropathy, including anterior horn lesions and peripheral neuropathy caused by various causes, **including **** and ****, anterior horn lesions of the spinal cord are most common in motor neuron disease and polio, there is currently no specific method for motor neuron disease, riluzole can be given orally, edaravone static point, and symptomatic support can be given at the same time**.

    Polio is currently prevented by oral vaccines, ** to acupuncture **** for the main finger, and nerve root compression or peripheral neuropathy caused by other causes can also cause muscle atrophy, such as the common Guillain-Barré syndrome, which is peripheral nerve damage caused by immune reasons, which can be given gamma globulin or plasma exchange, as well as autoimmune-mediated peripheral nerve damage due to other reasons, and hormones and immunosuppressants can also be used**. If it is due to compression by a tumor in the spinal cord or a herniated disc pressing on a nerve root, surgery may be given to relieve the compression. In addition, muscle atrophy can also be given acupuncture and ****.

  13. Anonymous users2024-01-31

    Motor neuron is a relatively rare degenerative neurological disease, which is so rare that even hospital doctors don't know much about it, so it is often difficult to diagnose it. Continental Fighting.

    Motor neuron is a disease characterized by progressive spinal muscular atrophy and amyotrophic lateral sclerosis, which is a progressive disease that progresses over time and has an increasing impact on life. When motor neurons are present, the more common early symptoms may be weakness and stiffness of finger movements, clumsiness of hand movements, and atrophy of hand muscles. Over time, it gradually expands to the forearms, pectoralis muscles, back, and even calves.

    Weakness of the limbs, muscle stiffness, difficulty moving, difficulty breathing and swallowing, and in severe cases, spastic paraplegia of the lower limbs may occur.

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