How to diagnose and differentiate progressive hemifacial atrophy?

summary

Progressive spinal cord atrophy, also known as progressive spinal muscular atrophy, is caused by the deformation of motor neurons in the anterior horn of the spinal cord and the motor nerves in the brain stem, resulting in the symptoms of muscle weakness, which will lead to muscle atrophy. It is mainly caused by the recessive genetic disease of chromosomes. It is not uncommon in clinic. How to diagnose and differentiate progressive hemifacial atrophy? Now let me tell you something.

How to diagnose and differentiate progressive hemifacial atrophy?

At present, there is no specific and effective treatment, through the prevention and treatment of various complications of myasthenia gravis, such as pneumonia or malnutrition, bone deformity and other movement disorders and some thorny social problems.

The emergence of such bacteria will lead to the integrity of the house, up and down will only be affected, to be able to develop rapidly, and the active movement of both lower limbs will be reduced, the surrounding muscles are very seriously affected, can not do alone, can not walk alone, will eventually develop to the hands and feet, only slight activity.

The patient's muscles will become sluggish, and muscle tension will be reduced, and muscle atrophy, in the limbs and neck to dry, but the chest muscles will bleed, and will lead to motor nerve damage, the average life expectancy is 18 months, generally in two years old, you will die.

matters needing attention

This kind of disease will have a series of complications, which will lead to muscle atrophy, dyspnea, hand and foot deformation. If it is serious, it will be due to severe pneumonia in 1898, so it will be life-threatening and there will be psychosocial problems, so we must treat it as soon as possible.