CLINICAL CASE OF AUTOSOMAL DOMINANT POLYCYSTOSIS OF THE KIDNEY IN A CHILD WITH CONNECTIVE TISSUE DYPLASIA

Abstract

The relevance of the problem of autosomal dominant polycystic kidney disease in childhood is due to age-related features of the formation of renal cysts and clinical manifestations, the frequent development of arterial hypertension syndrome and complications, and the outcome in chronic renal failure. The article presents a clinical case of a patient with autosomal dominant polycystic kidney disease. The peculiarity of this case is the proven hereditary nature of the disease, the presence of connective tissue dysplasia in the patient, the early manifestation of pathology in the form of renal hypertension. The use of the angiotensin-converting enzyme inhibitor losartan is an active pharmacotherapy for arterial hypertension and renoprotection in this patient.

Keywords

• дети
• аутосомно-доминантный поликистоз почек
• дисплазия соединительной ткани