Is Charcot Marie Tooth inherited in families?

Can Charoneal-Musular Dystrophy be inherited.

First, peroneal muscular atrophy is hereditary, about 80% of the disease is hereditary in families, and about 20% are sporadic; Most of them are close relatives who marry and have children. Most are inherited in an autosomal dominant manner.

Second, the pathological changes are mainly in the muscles and peripheral nerves. Muscle atrophy is mostly neurogenic atrophy, but myogenic atrophy may also be seen, or a combination of the two.

Peripheral nerves have pathological changes such as segmental demyelination, regeneration, axonal degeneration, myelopenia, and intraneural connective tissue hyperplasia.

Third, the disease is caused by a hereditary defect in Schwann cells or axons in peripheral nerves, which in recent years is thought to be related to immunity. Patients may have imperfect thymus and intestinal immune mechanisms, allowing certain exogenous substances such as lentivirus to invade genetically predisposed individuals through the intestinal mucosa and cause disease.

Precautions. Peroneal muscle atrophy is an inherited progressive peripheral neuropathy. **Unknown, more common in men than women, the most common symptoms are early slow running, weakness and atrophy of the peroneal, extensor digitorum longus, and minor muscles of the foot.

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.

Depending on the location of the lesion, ataxia can be divided into four types: deep sensory impairment ataxia; cerebellar ataxia; vestibular labyrinthine ataxia; Cerebral ataxia. The commonly known as "ataxia" refers to cerebellar ataxia.

The accurate completion of any movement requires the close coordinated participation of the muscles that play an active, synergistic, antagonistic and fixed role in different stages of the movement. It is usually divided into four types: cerebellar ataxia, sensory ataxia, vestibular ataxia, and cerebral ataxia according to the location of the lesion.

Ataxia is a neurological disorder that is controlled by recessive genes and is somewhat hereditary. Ataxia has many harms to oneself and affects the normal state of life. Once the symptoms of ataxia are found, we must pay attention to it and go to a regular professional hospital for examination as soon as possible** to avoid delaying the condition and reducing the harm of the disease to ourselves.

I don't know if you have noticed some phenomena: some people walk unsteadily and cannot walk in a straight line; Some people struggle to balance their bodies, but still stagger, leaning forward and backward; gait disorder, easy to fall; Poor mental state, sluggishness, etc. In this regard, it may be ataxia.

We can't laugh it off, we must pay attention to it. So, what is ataxia?

Ataxia is a condition that arises as a result of damage to a part of the nervous system. As a result, the person's motor coordination difficulties, balance problems, etc. The former is called dynamic ataxia, and the latter is called static ataxia.

Depending on the site of the lesion, we can divide it into four types: cerebellar ataxia, cerebral ataxia, vestibular labyrinthine ataxia, and deep sensory impairment ataxia. When we talk about ataxia, we generally refer to cerebellar ataxia.

There are many types of ataxia, including cerebellar lesions and peripheral neuropathy. There are also some factors that are unexplained, and the situation will be more complicated. Patients should go to the neurology department of a specialized hospital to determine **, symptomatic ** is the best choice.

If it can be cured, you have to believe in medicine. I heard that there are a lot of **methods now.,But it's recommended to choose the best **method for yourself.,You can ask the doctors in the early stage.,Let the doctor help you choose.,Haha。。

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Patients with peroneal muscular atrophy should avoid forced functional exercises, because forced functional exercises can lead to skeletal muscle fatigue, which is not conducive to the recovery of skeletal muscle function and the regeneration and repair of muscle cells. Intense long-term or repeated emotional changes, such as stress, anxiety, boredom, pessimism, etc., can lead to an imbalance in the excitatory and inhibitory processes of the cerebral cortex, aggravate muscle jumps, and develop muscle atrophy.

Charoneal-muscar-atrophy is currently not special**, mainly symptomatic **and supportive**. People with pendulous feet or foot deformities can wear orthopedic shoes. Drugs** can be used to promote the regeneration of diseased nerve fibers with vitamins, and neuromuscular nutrition drugs can also help.

Acupuncture and physiotherapy, as well as exercises and massage of the muscles and Achilles tendons, can enhance their telescopic function. Foot drops can be corrected, such as wearing high heels, boots, or corrective shoes, and severe ankle contractures can be surgically released or tendon grafted. Patients should not overexert themselves and should pay attention to keeping warm.