Clinical cases of hereditary nephropathy among children in Andijan region

Автор: Ganieva M.Sh., Efimenko O.V., Rakhmanova L.K., Boltaboeva M.M., Majidova N.M.

Журнал: Экономика и социум @ekonomika-socium

Рубрика: Основной раздел

Статья в выпуске: 2-1 (93), 2022 года.

Бесплатный доступ

Congenital pathology of the urinary system often develops latently, progresses without pronounced extrarenal manifestations and attracts attention only with the development of symptoms of renal failure. A marker of hereditary and congenital diseases of various organs and systems, including the kidney, is the presence of stigmas of connective tissue dysembryogenesis or minor developmental anomalies. Issues of timely diagnosis can enable early correction of homeostasis disorders that develop as a result of renal failure, rationally carry out renoprotection.

Hereditary nephropathy, fanconi nephrophthisis, lowe's syndrome, alport's syndrome

Короткий адрес: https://sciup.org/140291056

IDR: 140291056

Статья научная