The diagnosis of facial paralysis primarily relies on the patient’s symptoms, including stiffness of the facial muscles and distortion of the mouth and eyes. The possible causes are numerous, and treatment involves not only nourishing the nerves but also addressing the underlying disease.
The cost of facial paralysis treatment and the best treatment methods
A four-month-old baby is showing signs of iron deficiency, with no weight gain and recent diarrhea. How can iron supplementation and growth improvement be achieved?
How to diagnose and provide treatment recommendations for hand, foot, and mouth disease
While fever medication can alleviate symptoms, excessive use may harm your body. It is recommended to use it under a doctor’s guidance and follow the dosage instructions on the medication label.
For children who may have epilepsy from birth and whose condition has progressed to monthly or even multiple monthly seizures, they are currently undergoing treatment with Depakene and Tegretol, but the effect is not satisfactory. It is suggested to try carbamazepine treatment and consider going to a specialized epilepsy hospital for examination to assess whether surgery is suitable. At the same time, the importance of seeking timely treatment at professional hospitals for regular treatment is emphasized to avoid the deterioration of the condition.
How to treat and control the blood phenylalanine concentration in children with phenylketonuria?
If a newborn’s facial features suggest Down syndrome, how should the diagnosis and care be handled?
The child has been coughing for a month, and despite taking prescribed cough medicine, there has been no improvement. Suddenly, the child developed a high fever yesterday, which subsided after receiving intravenous drip treatment, but the coughing persists. The doctor checked the trachea and throat and found no abnormalities. Inquire about the cause and dietary precautions.
Down syndrome, also known as trisomy 21, is a disorder caused by chromosomal abnormalities. The risk is higher for older mothers, and it is recommended that both partners undergo chromosomal testing. If no abnormalities are found with chromosome 21, theoretically, they can consider having another child.
