[1] Bergmann, C., Guay-Woodford, L. M., Harris, P. C., Horie, S., Peters, D. J. M., & Torres, V. E. (2018). Polycystic kidney disease. Nature Reviews. Disease Primers, 4(1), 50. https://doi.org/10.1038/s41572-018- 0047-y
[2] Loftus, H., & Ong, A. C. M. (2013). Cystic kidney diseases: Many ways to form a cyst. Pediatric Nephrology, 28, 33–49. https://doi.org/10.1007/s00467-012- 2221-x
[3] Dell, K. M. (2015). The role of cilia in the pathogenesis of cystic kidney disease. Current Opinion in Pediatrics, 27(2), 212–218. https://doi.org/10.1097/MOP.0000000000000187
[4] Medscape. (2021). Cystic diseases of the kidney clinical presentation. https://emedicine.medscape.com/article/453831- clinical
[5] Hill, N. R., Fatoba, S. T., Oke, J. L., Hirst, J. A., O’Callaghan, C. A., Lasserson, D. S., & Hobbs, F. D. R. (2016). Global prevalence of chronic kidney disease - A systematic review and meta-analysis. PLoS One, 11(7), e0158765. https://doi.org/10.1371/journal.pone.0158765
[6] Nardiello N, A., Lagomarsino F, E., Baquedano D, P., & Aglony I, M. (2007). Quistes renales, manifestación de diversas patologías. [A clinical approach to renal cysts]. Revista Medica de Chile, 135(1), 111–120. https://doi.org/10.4067/S0034- 98872007000100016
[7] Pohl, M., Bhatnagar, V., Mendoza, S. A., & Nigam, S. K. (2002). Toward an etiological classification of developmental disorders of the kidney and upper urinary tract. Kidney International, 61(1), 10– 19. https://doi.org/10.1046/j.1523-1755.2002.00086.x
[8] Ali, T. M., Abdelraheem, M. B., Mohamed, R. M., Hassan, E. G., & Watson, A. R. (2009). Chronic renal failure in Sudanese children: Aetiology and outcomes. Pediatric Nephrology, 24(2), 349–353. https://doi.org/10.1007/s00467-008-1022-8
[9] Abdalrahman, I. B., Elgenaid, S. N., Ellidir, R., Abdallah, A. N. M. O., Hamid, S. A. H., Elwidaa, S. H. A., & Ali, E.-T. M. A. (2019). Breaking the bottle neck to enhance pediatrics renal transplantation at Soba university hospital: Role of a non-governmental organization. Healthcare in Low-Resource Settings, 7(1). https://doi.org/10.4081/hls.2019.7930
[10] Levey, A. S., Eckardt, K. U., Tsukamoto, Y., Levin, A., Coresh, J., Rossert, J., De Zeeuw, D., Hostetter, T. H., Lameire, N., & Eknoyan, G. (2005). Definition and classification of chronic kidney disease: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO). Kidney International, 67(6), 2089–2100. https://doi.org/10.1111/j.1523- 1755.2005.00365.x
[11] Kurschat, C. E., Müller, R. U., Franke, M., Maintz, D., Schermer, B., & Benzing, T. (2014). An approach to cystic kidney diseases: The clinician’s view. Nature Reviews. Nephrology, 10, 687–699. https://doi.org/10.1038/nrneph.2014.173
[12] Sigmon, D. F., Shikhman, R., & Nielson, J. l. (2023). Renal cyst. Stat Pearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK470390/
[13] Spence, H. M. (1955). Congenital unilateral multicystic kidney: An entity to be distinguished from polycystic kidney disease and other cystic disorders. The Journal of Urology, 74(6), 693–706. https://doi.org/10.1016/S0022-5347(17)67338-5
[14] Ghata, J., & Cowley, B. D., Jr. (2017). Polycystic kidney disease. Comprehensive Physiology, 7(3), 945–975. https://doi.org/10.1002/cphy.c160018
[15] Marie Patrice, H., Joiven, N., Hermine, F., Jean Yves, B., Folefack François, K., & Enow Gloria, A. (2019). Factors associated with late presentation of patients with chronic kidney disease in nephrology consultation in Cameroon – A descriptive crosssectional study. Renal Failure, 41(1), 384–392. https://doi.org/10.1080/0886022X.2019.1595644
[16] Barbari, A., Stephan, A., Masri, M., Karam, A., Aoun, S., El Nahas, J., & Bou Khalil, J. (2003). Consanguinity-associated kidney diseases in Lebanon: An epidemiological study. Molecular Immunology, 39(17-18), 1109–1114. https://doi.org/10.1016/S0161-5890(03)00065-8
[17] Mattoo, T. K. (1998). Genetically transmitted renal diseases in children: A Saudi perspective. Saudi Journal of Kidney Diseases and Transplantation, 9(2), 105–109.
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