How to Treat Congenital Kidney Disease in Children?

The treatment methods for congenital kidney disease in children mainly include the use of corticosteroids (such as prednisone, prednisolone, etc.), cytotoxic drugs (cyclophosphamide), or immunosuppressants (cyclosporine A, tacrolimus, mycophenolate mofetil, leflunomide, etc.). Other possible measures for reducing urine protein levels include traditional Chinese medicine such as thunderbug vine and immunostimulants. If a child is troubled by pediatric kidney disease syndrome, mothers must take their children to the doctor immediately for treatment, avoid blind use of small advertisement drugs, and ensure rational medication. For parents, it is crucial to keep a close eye on their child’s condition to help them receive timely treatment for the disease.
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Symptoms of Pediatric Kidney Disease

The symptoms of pediatric kidney disease syndrome include the following: 1. Pediatric kidney disease often occurs in children aged 2 to 6, with a significantly lower incidence in boys compared to girls. Children with kidney disease tend to develop and delay symptoms, usually within a month after infection. 2. Children with kidney disease may experience facial, trunk, and lower limb edema in the early stages, with eyelid edema being the most typical and common initial symptom of kidney disease in children. Severe cases may also involve skin thinning, ascites, and pleural effusion.
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