Nephropathy Endemic Balkan

Endemic Balkan nephropathy: causes, symptoms and treatment

Endemic Balkan nephropathy, also known as Balkan nephritis, is a chronic kidney disease that is usually observed in people living in regions of the Balkan Peninsula. This disease is characterized by damage to the kidneys, which leads to progressive loss of kidney function and ultimately to chronic renal failure.

Causes

The causes of Endemic Balkan nephropathy are still not fully understood. However, scientific research has shown that the disease may be associated with long-term exposure to various factors, including:

  1. Consumption of drinking water contaminated with heavy metals, especially cadmium and lead.
  2. Consumption of foods grown in soils contaminated with heavy metals.
  3. Frequent use of analgesics and non-steroidal anti-inflammatory drugs.

Symptoms

Endemic Balkan nephropathy can present with a variety of symptoms, which include:

  1. High blood pressure.
  2. Edema.
  3. Lower back pain.
  4. Urination, accompanied by pain and changes in the color of urine.
  5. Deterioration in general health.

Treatment

Treatment of Endemic Balkan nephropathy should be comprehensive and include several stages. First of all, it is necessary to exclude exposure to factors on the body that can lead to disease. It is recommended to use special water purification systems and consume products grown on environmentally friendly soils.

It is also important to have regular medical check-ups and take steps to control your blood pressure and maintain normal blood sugar levels. If necessary, it may be necessary to prescribe drug therapy aimed at maintaining kidney function.

In conclusion, Endemic Balkan nephropathy is a serious disease that requires comprehensive and timely treatment. At the first signs of the disease, you should consult a doctor and begin the process of diagnosis and treatment.



Balkan endemic nephropathy (EBF) is a chronic inflammatory kidney disease caused by infection with group A beta-hemolytic streptococcus. The syndrome is a type of pastoral subacute glomerulonephritis, more or less associated with bacterial pathology of the ENT organs and diseases of the oral cavity. In this nosoform, nephroitis does not appear from distant foci of hemolysis, with the exception of the mentioned contingent of elderly people with unchanged kidney function. This is one of the simplest forms of glomerulopathies, characterized by a significant number of predisposing factors, an asymptomatic course and low proteinuria, as well as a relatively favorable prognosis compared to glomerulopathies caused by the Coxsackie virus and other viruses. In other words, this disease has few symptoms, is malignant, leads to renal failure and can cause complications such as renal infarction. Mostly children and adolescents suffering from tonsillitis, scarlet fever, stomatitis, and tonsillitis are susceptible to the disease. When glomerular changes appear in the acute stage, they are observed much more often than when they are detected 3 weeks after the onset of the disease. In those who have recovered from a streptococcal infection, if it appears during a period when the disease is already