肌萎缩性脊髓侧索硬化症的中医治疗(国外英文资料).docVIP

肌萎缩性脊髓侧索硬化症的中医治疗(国外英文资料) TCM treatment of als with als Yang xiaoheng, a hospital in yizhang county, hunan province Amyotrophic lateral sclerosis (ALS) is the most common in motor neuron disease. More men than women start after age 40; Pathological changes mainly involving the cerebral cortex motor area, pyramidal tract, brainstem cranial nerve motor nucleus and spinal cord, such as upper and lower motor neuron of anterior horn cells, so in upper and lower movement characteristic of the nerve damage to coexist. The anterior cervix cells of the cervix are often tired, and the spinal cord of the cortex is also affected. The first symptom is a two-sided hand that is incapable of clumsiness, and gradually appears muscle atrophy, which is marked by the size of the interfish muscle and the lumbril muscle, which is a clawed hand. Muscle weakness and atrophy are gradually extending to the forearm and shoulder, and the lesion has a wide and distinct pulsating muscle. The upper extremities, which are often pronounced in the muscle, are pronounced in the musculus, the interosseous muscle and the lumbar muscle. However, due to the damage of the cone, the increase of muscle tension, hyperactivity of tendon reflex, and pathological signs are positive. When the motor nerve does not have severe damage, the conical bundle symptoms are covered, the upper extremity muscle tension decreases, the tendon reflex decreases or disappears. The lower limbs are more spasmodic, the muscle tension increases, the tendon reflexes, and the pathologic reflection occurs. The lower extremity muscle atrophy and muscle pulsations are lighter or less obvious. When the ball is paralyzed, the hyoid muscles atrophy and vibrate, but the lower jaw reflexes, showing the combined damage of the upper and lower motor neurons. There is usually no sphincter dysfunction. A small number of cases have been raised from the lower extremities, which are gradually extended and the upper limbs. It can be subjective, such a