Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)

Congenital anomalies of the kidney and urinary tract (CAKUT) occur in 0.5–1/100 newborns and as a group they represent the most frequent cause for chronic kidney failure in children. CAKUT comprise clinically heterogeneous conditions, ranging from mild vesicoureteral reflux to kidney aplasia. Most f...

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Veröffentlicht in:	Molecular and Cellular Pediatrics 2021-02, Vol.8 (1), p.2-2, Article 2
Hauptverfasser:	Kohl, Stefan, Habbig, Sandra, Weber, Lutz T., Liebau, Max C.
Format:	Artikel
Sprache:	eng
Schlagworte:	Animal models Aplasia Chronic kidney failure Congenital defects Development and progression Diabetes Endocrinology Etiology Genetic disorders Genetic diversity Genetic engineering Kidneys Medical research Medicine Medicine & Public Health Medicine, Experimental Mesenchyme Mini Review Neonates Oncology Pediatrics Renal failure Rodents Transgenic mice Ureter Urinary tract Urogenital system
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