Treatment for a child’s cough should first identify the cause, common medications include Feilike cough mixture and Chuanbei Pipayao, but attention should be paid to symptomatic treatment, and for severe or persistent coughs, relevant examinations should be conducted.
Phenylketonuria is a genetic amino acid metabolic deficiency disease, with an autosomal recessive inheritance pattern.
For the treatment of pediatric cough and cold, it is recommended to follow the doctor’s guidance, including oral medication or intravenous fluid therapy, and pay attention to prevent complications such as bronchitis and pneumonia. At the same time, ensuring the child drinks plenty of water, stays warm, and consumes appropriate dietary supplements can help in the recovery of the illness.
If a child can’t breathe through their nose at night and has yellow phlegm in the morning, it might be due to a respiratory infection. How should it be handled?
The examination project for pediatric cerebral palsy includes electrophysiological tests such as EEG, BEAM, brain magnetic resonance imaging, and evoked potentials to assess brain function and pathological conditions.
A cough caused by adenoid hypertrophy in children may be due to tonsillitis, which is an acute infection of the upper respiratory tract, often accompanied by acute inflammation of the pharyngeal mucosa and tonsil lymphoid ring. Treatment may consider the use of antibiotics for intravenous injection.
If a baby has a runny nose and phlegm in the throat, it may be due to bronchitis caused by a cold. It is recommended to take medication under a doctor’s guidance and pay attention to adequate hydration and rest.
Pediatric nephritic syndrome should first identify the cause, which is commonly due to family hereditary diseases, congenital kidney disease complex, or primary glomerulonephritis. Excluding the first two causes, primary glomerulonephritis is considered first. The nephrotic syndrome caused by primary glomerulonephritis in children is mainly characterized by microscopic changes in pathology, with clinical manifestations of simple massive proteinuria without hematuria, which can be diagnosed through clinical symptoms and signs. Treatment mainly involves the use of corticosteroids to suppress immune-inflammatory reactions. Microscopic change type kidney disease is relatively sensitive to corticosteroid treatment, with good effects, and most cases can turn urine protein negative within a month.
Common abdominal pain and nausea after meals in children may be caused by gastritis, and attention should be paid to diet and medication treatment.
If a baby is infected with the hand, foot, and mouth disease virus, parents should take the child to the hospital for immediate treatment. Under the guidance of a doctor, use antiviral medications for treatment and pay attention to the child’s body temperature changes. Additionally, maintaining good personal hygiene habits, ensuring a balanced diet for the baby, and frequently measuring body temperature and replenishing fluids are all necessary care measures.
