Abstract
Congenital anomalies of the kidney and urinary tract (CAKUT spectrum) affect up to 3% of human fetuses, and they present major diagnostic and management challenges to practising physicians. In order to frame the clinical implications of CAKUT, it is critical to understand the normal development of the kidney and urinary tract. Although accounts on pathogenesis focus predominantly on genetic causes of CAKUT, it is also important to consider other contributing factors such as lower urinary tract obstruction, teratogens, and maternal diet. In this chapter, we will discuss the anatomy, embryology, and pathogenesis of CAKUT.
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Abbreviations
- CAKUT:
-
Congenital anomalies of the kidney and urinary tract
- CKD:
-
Chronic kidney disease
- MCDK:
-
Multicystic dysplastic kidney
- PKD:
-
Polycystic kidney disease
- RCAD:
-
Renal cysts and diabetes syndrome
- UPJ:
-
Ureteropelvic junction
- UVJ:
-
Ureterovesical junction
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Al-Harbi, A., Winyard, P. (2016). Anatomy, Applied Embryology, and Pathogenesis of Congenital Anomalies of the Kidney and Urinary Tract. In: Barakat, A., Rushton, H. (eds) Congenital Anomalies of the Kidney and Urinary Tract. Springer, Cham. https://doi.org/10.1007/978-3-319-29219-9_2
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DOI: https://doi.org/10.1007/978-3-319-29219-9_2
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