Abstract
Tug‘ma va irsiy buyrak kasalliklari bolalar va o‘smirlarda surunkali buyrak kasalligi (SKD) hamda buyrak yetishmovchiligining muhim sabablaridan hisoblanadi. Ushbu tezisda buyrak va siydik yo‘llarining tug‘ma anomaliyalari (CAKUT), Alport sindromi,
autosom-dominant va autosom-retsessiv polikistoz kasalliklar kabi holatlarda SKD rivojlanish va progressiya xavfini baholash mezonlari tahlil qilindi. Xavfni stratifikatsiya qilishda glomerulyar filtratsiya tezligi (eGFR), albuminuriya/proteinuriya, arterial gipertenziya, takrorlanuvchi siydik yo‘li infeksiyalari, obstruktiv uropatiya, buyrak parenximasi displaziyasi, oilaviy anamnez va genetik variantlar muhim prognostik omillar sifatida ko‘rib chiqildi.
References
1. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. (2024). KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney International, 105(Suppl. 4S), S117–S314.
2. Levin, A., et al. (2024). Executive summary of the KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney International, 105, 684–701.
3. Stonebrook, E., Hoff, M., & Spencer, J. D. (2019). Congenital anomalies of the kidney and urinary tract: A clinical review. Current Treatment Options in Pediatrics, 5(3), 223 235. https://doi.org/10.1007/s40746-019-00166-3
4. Yosypiv, I. V. (2023). Congenital anomalies of the kidney and urinary tract: Defining risk factors of disease progression and determinants of outcomes. Pediatric Nephrology.
5. Wood, E. G., et al. (2022). Urologic considerations in pediatric chronic kidney disease. Advances in Chronic Kidney Disease, 29(3), 250–259.