Is a relatively rare baby's kidney disease, but once the consequences of serious illness. Congenital nephrotic syndrome is about 3 to 6 months after the onset of a kidney disease, it has four major characteristics of nephrotic syndrome:
Can Children Suffer from Nephrotic Syndrome
① a large number of proteinuria, qualitative examination ≥ (+++), quantitative daily o.1g / kg;
② low proteinemia, serum albumin <3g / L;
③ hypercholesterolemia, serum cholesterol more than 5.72mmol / L;
④ edema. Congenital nephrotic syndrome is divided into primary and secondary,
What is Permanent Solution for Nephrotic Syndrome In Children
Primary is the main type of congenital nephrotic syndrome in Finland,
Secondary type can be secondary to infection (such as congenital syphilis, giant cell inclusion body virus, rubella, hepatitis), poisoning, hemolytic uremic syndrome.
Prognosis of Nephrotic Syndrome in Children
Finnish congenital nephrotic syndrome is an autosomal recessive inheritance, children often premature children, a large placenta, nasal small, low nose, eyes wide, poor muscle tension. Born with proteinuria, edema and ascites soon, and often umbilical hernia, children feeding difficulties, easy to vomit and diarrhea, growth retardation, some children may be hypercoagulable state, leading to thrombosis complications. Early normal renal function, but susceptible to infectious diseases. The disease without specific treatment, only symptomatic and supportive therapy, prevention and treatment of infection, reduce edema, steroids and immunosuppressive agents invalid. The poor prognosis of this disease, more than 6 months to 1 year old died of infection, such as to survive to 2 to 3 years old often died of uremia. So the most thorough treatment is 2 years of age after renal transplantation.
How to Avoid Relapse in Nephrotic Syndrome for a 5 Year Old Boy
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