Pseudohypertrophic myotonic dystrophy can be treated as follows, and this protocol has been observed in recent years to have improved and improved the clinical symptoms in many patients. Early treatment usually delays the progression of the disease for more than 5 years, and we are pleased to find that many patients are not paralyzed at the age of 12 and can continue to walk. Each of the following measures can be found reported in the literature at Pubmed. There is no better treatment than this program, but you have to visit your doctor where you can get a good grasp of the situation and design a treatment plan based on your child’s specific situation, as to how to implement it and what side effects to pay attention to. 1, first of all, we must face the reality and full of confidence, life is short, must live a happy and meaningful. 2, to protect the muscles, overtraining aggravates the development of the disease, the damage to the muscles of the disease and activities have a close relationship, the more activities, the heavier the damage. (1) bicycle substitute can prevent muscle cost atrophy, the sooner the better. Once lying down, the muscle rapidly atrophies and can never get up. (2) muscle exists in the physiological ischemic state of muscle infarction changes, do not stand and walk for a long time, interval 20-30 minutes moderate limb relaxation and massage may be improved. (3) Protect the easily damaged muscles, use thick sponge cushion in sitting position to protect the gluteus muscle; add external force to the outer thigh in sitting position to make the legs passively come together to protect the large collecting muscles; do not go up or down stairs to protect the quadriceps muscle. (4) Warm water bathing is good for the muscles. 3, low protein high fat diet, do not over-nutrition, fat accelerates the development of the disease, our research has confirmed that weight below 10% of the normal average is good (plus or minus 30% of the standard weight is the normal range). In addition to control the amount of salt, more sodium in the muscle fibers aggravate the development of the disease. Drink green tea every day. 4, carry out moderate rehabilitation to prevent Achilles tendon contracture. Wearing corrective shoes can improve the child’s abnormal walking posture, and studies have confirmed that no treatment is better than wearing corrective shoes. However, moderate activity is required. 5.Medication (1) Glucocorticoid, 0.75 mg/kg/day. The disease is an inflammatory muscle damage caused by a genetic mutation. Studies have proven that starting with it at the age of 2-4 years old, with calcium and potassium, it is the best drug treatment available and can greatly delay the development of the disease. Obese children take 0.3 mg/kg/day. Aspirin also has an anti-inflammatory effect, but the dose is too high for the child to use for a long time. (2) Addibenzoquinone, studies have proven that high doses, used on the basis of hormone therapy to improve muscle strength by 8%, cannot be used alone. (3) Salbutamol, studies have proven that it can increase the amount of an anti-muscle atrophy protein substitute on the muscle fiber membrane and increase muscle strength. Gentamicin also has this effect, but the side effects are too great for long-term use. (4) Eplerenone at doses of 25-50 mg/day for children and 50-100 mg/day for adults. Take these drugs to reduce sodium in muscle fibers, thus reducing edema and slowing the progression of the disease, the drug is not available in China and is replaced by hesperidin. (6) arginine, the drug is effective (1g qd), elevated nitric oxide and act to increase muscle strength, reduce muscle steatosis and fibrosis, morindaine (1mg. bid) has the same effect. (7) L-carnitine, stabilizes the lipid membrane of muscle fibers and has a protective effect (8) Appropriate use of testosterone, the child with onset has gonadal damage and low testosterone, which can be appropriately supplemented for the purpose of strong muscles. (9) The child should be regularly observed for heart and lung function after the age of 7.