Urinary occult blood in children with Alport syndrome usually fails to turn negative.
Alport syndrome, a genetic mutation caused by hereditary kidney disease, the main clinical manifestations of hematuria, proteinuria, etc., and may or may not be accompanied by sensorineural deafness, eye lesions. Because Alport syndrome is a genetic lesion, there is no specific treatment, therefore, Alport syndrome caused by children’s urinary occult blood usually can not turn negative.
In addition, children should pay attention to rest, avoid exertion and infection, and prohibit nephrotoxic drugs. Hydrochlorothiazide and furosemide can be used to relieve symptoms when edema occurs. If necessary, kidney transplantation is also needed for treatment.
In life, children with Alport Syndrome should control their diet, focusing on high-quality and low-protein diets, and actively cooperate with the doctor’s treatment, and immediately consult a doctor if they feel unwell. The above drugs should be used according to the doctor’s prescription.