Treatment Methods for Facial Paralysis Post-Stroke Muscle Atrophy

Facial paralysis post-stroke muscle atrophy refers to the condition where the disease has not healed after three months, which can be categorized into central and peripheral types, caused by factors such as infection, trauma, poisoning, and metabolic disorders. The main symptoms include facial muscle paralysis, where patients may suddenly find one side of their face unresponsive during morning facial washing, with the mouth drooping. Other symptoms include the disappearance of forehead wrinkles, widened eye fissures, flattened nasolabial grooves, and protruding corners of the mouth, with the mouth corner tilting towards the healthy side when showing teeth. The treatment methods for post-stroke muscle atrophy vary depending on the location and are more challenging to treat.
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Treatment Methods for Facial Paralysis Sequelae

The treatment for facial paralysis Sequelae primarily focuses on restoring activity functions as completely as possible and avoiding colds, wind, and facial exposure to chill. It is recommended to stay away from computers, televisions, and ultraviolet radiation, avoid spicy and irritating foods, maintain a light diet and a relaxed mood, and actively participate in sports to regulate physical and mental health and maintain personal hygiene.
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Treatment Methods for Facial Paralysis with Neurotrophin

Facial paralysis can be categorized into central and peripheral types. The former is usually caused by central nervous system diseases, while the latter is often idiopathic facial paralysis, with treatment methods varying according to the underlying cause. Neurotrophin can be used as an adjunct in the treatment of facial paralysis, but professional medical advice should be sought before use.
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