Abstract:
. In order to identify clinical and genetic risk factors for the development of hereditary nephritis in children, data from 168 medical histories of children aged 1 to 14 years with a diagnosis of glomerulonephritis (acute-130 and chronic-38) for 2017-2021 were analyzed. Who received inpatient treatment in the children's multidisciplinary clinic of Andijan State Medical Institute. It was revealed that in the conditions of the Fergana Valley there is a tendency to increase the number of patients with urinary tract infection and dysmetabolic nephropathies of familial genesis. The incidence of hereditary nephritis is higher among patients with chronic
glomerulonephritis than with acute glomerulonephritis and pyelonephritis. Algorithms for early diagnosis of hereditary nephritis in children include combined damage to the organs of hearing and vision, kidney diseases in several family members or among relatives.
