Multiprofile Department of Rare Diseases

The Evex Department of Rare Diseases includes several services: nephrology, endocrinology, neurology, hematology, rare and genetic diseases. Diagnosis and management of the following diseases are carried out in the department:

Nephrology

• acute nephritic syndrome;
• idiopathic nephrotic syndrome;  
• chronic nephritic syndrome (primary and secondary);
• complicated and uncomplicated urinary tract infections (developed congenital anomalies, neuromuscular dysfunction of urinary bladder);
• acute tubulointerstitial nephritis; 
• acute and chronic renal failure;
• inherited nephropathy;

• rare diseases:
  • various types of tubulopathy.

  Neurology:

• epilepsy;  
• neuroinfection;
• neurocranium trauma;
• brain blood circulation disorders;
• chronic neurological diseases;

• rare diseases:
  • congenital metabolic diseases of nervous system;
  • neuromuscular diseases.

 Hematology

• deficiency anemia (iron and vitamin deficiency);
• primary red cell aplasia
• idiopathic thrombocytopenic purpura;
• rare diseases:
  • inherited blood diseases (thalassemia, microspherocytosis, fermentopathy).  

 Endocrinology

• Type I diabetes;
• Type II diabetes;
• hypoglycemia;
• thyroid gland diseases (toxic goiter);
• adrenal gland diseases (Addison’s disease).

Rare genetic diseases

• cystic fibrosis;
• incomplete osteogenesis;
• Bruton’s disease.