Is muscle wasting hereditary?

Muscle wasting (ALS) is not a genetic disorder, so there is no need to worry about it.

ALS is known to be a type of motor neuron diseaseALS is sporadic in clinical practice, and it is a rare disease in itself, and only a small number of patients have familial diseaseTherefore, during the course of the disease, if there are several patients in the family who have such conditions, genetic screening may be done in related aspects.

However, for the vast majority of patients, it is currently thought to be sporadic, possibly related to viral infection or genetic changes, and so far no specific virus or genetic changes have been found. That is to say, ALS itself is an individual disease and is not a genetic disease. So you don't need to worry about ALS being passed on to your children, because that's not how it is transmitted.

I know a patient with ALS, of course, he is still in the early stage, so there will not be too many restrictions on his movements, but everyone knows how the disease will develop in the end, so the people around him still take good care of him.

And this is the only one person I know of ALS, and no one in their family has ever had it. At least his parents, elders, and the like, have no corresponding illnesses, and his children are also very healthy people. Let's not explain it scientifically, just use the family situation we have observed, and we can see that this disease should not be a genetic disease.

Of course, the research on ALS is still relatively shallow, but it is certain that for the vast majority of people, ALS is not hereditary, but the specific pathological mechanism is still not very clear, everyone only knows that he can have atrophy of nerve cells, necrosis and other conditions, but what is the reason for this? Can it be expected to strangle it in the cradle? None of these issues have been well resolved.

However, it is believed that with the development of science and the improvement of medical level, ALS will also become a disease that can be used in the future. As for what pathology causes ALS, at least it has not been found to be related to genetics.

The reason why everyone is so different about ALS is that on the one hand, it will bring very terrible physical changes to people, and on the other hand, it is also because everyone is not familiar with this disease. Although through some news reports, everyone has more or less some understanding of ALS, but what causes this disease and whether it will be inherited is still a deep confusion in everyone's heart. Most of the current medical studies have shown that ALS is not hereditary, it is just an isolated case.

Amyotrophic lateral sclerosis, also known as motor neuron disease (MND) or ALS, is caused by damage to upper and lower motor neurons, resulting in gradual weakness and atrophy of muscles including the bulbar (the part of the muscles innervated by the medulla), limbs, trunk, chest, and abdomen.

What are the symptoms of muscle atrophy, and is there a difference between ALS?

Muscle wasting is not necessarily a condition of ALS.

Muscle atrophy can be caused by damage to simple muscles or damage to local muscle-nerve junctions and the nerves innervating muscles, such as lower limb muscles, due to pain, numbness, and atrophy caused by lumbar disc herniation compressing nerve roots. ALS, on the other hand, affects upper and lower motor neurons due to the hardening of the lateral cords, which is not limited to local, which is the difference in the site of occurrence of the two.

Secondly, in terms of symptoms, muscle atrophy is simply the inflexibility of damaged muscles, thinning and weakness, etc., while ALS will first appear clumsiness of the fingers, and later affect the muscles in many parts of the body, including severe atrophy of the ventilator.

Third, the effect of muscle atrophy is generally better, and after exercising including removing some damage, it can restore function and local muscle strength, while the effect of ALS is generally not particularly ideal.

ALS, also known as amyotrophic lateral sclerosis, is a type of motor neuron disease that manifests as peripheral paralysis involving upper and lower motor neurons.

In the early stages of ALS, symptoms such as sudden falls and loss of exercise ability may occur, and as the disease progresses, muscle atrophy to varying degrees may occur, and finally breathing disorders may occur.

ALS is also known as one of the "five rare diseases in the world", because its pathogenesis is not yet clear, it can only be maintained with drugs such as Xieyili riluzole tablets, so as to delay the time of breathing disorders as much as possible, and then delay the tracheostomy time.

At present, there is no practical method for muscle atrophy for patients with ALS, and recovery is unlikely.