Nephrosis Familial

Familial nephrosis is a disease in which the kidney tissue is modified due to the inflammatory process. The most common form is focal: there are limited areas of thinning of the parenchyma. Basically, this is an isolated lesion of any one kidney. Nephrosis is not a separate disease, but rather a pathological change in kidney tissue that develops in connection with the impact of certain factors on the body. At the initial stages, changes in the kidneys are reversible, and as the functioning of systems and organs improves, inflammation subsides, decreases, and tissue changes disappear. But the recovery period may be long, or may be absent altogether. Each stage of the disease has its own characteristics that make it possible to differentiate nephrosis of different stages. Among the causes of the development of the disease are autoimmune diseases with increased levels of hepatic factor (Wegener's granulomatosis, infectious mononucleosis), malformations of the vessels of the renal arteries, vasculitis, etc. Symptoms may include increased body temperature, fatigue, weakness, lower back pain, etc. Treatment of nephrosis carried out in the same way as during other diseases accompanied by kidney changes. Usually the disease can continue even after kidney surgery or kidney replacement. The prognosis and consequences are extremely unfavorable for a sick person.