Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) are developmental abnormalities present from birth. These conditions affect the structure or function of the kidneys or urinary tract and are among the most common causes of chronic kidney disease in children. Some of the common anomalies include kidney malformation, obstruction in urine flow, vesicoureteral reflux (backflow of urine), and duplicated urinary systems. Early diagnosis and proper management are essential to protect kidney function and ensure normal growth and development. Our approach focuses on accurate evaluation, timely treatment, and long-term follow-up to keep the kidneys functioning well.
Congenital kidney or urinary tract conditions may be detected before birth or become noticeable later in childhood. They may be suspected in the following situations:
Since these are developmental conditions, the kidneys or urinary tract may not form or function normally. Depending on the type of anomaly, this can lead to:
Treatment depends on the type and severity of the anomaly. The aim is to protect kidney function, prevent infections, and ensure normal development. Management may include:
Early detection allows timely intervention and helps preserve kidney health. With proper care, children can lead normal, healthy lives. Benefits include:
Parents should consult a specialist if any abnormal signs appear in infants or children. Immediate evaluation is advised if you notice:
Congenital anomalies of the kidney and urinary tract require careful evaluation and long-term care. With the right diagnosis, appropriate treatment, and regular monitoring, most children can maintain good kidney function and enjoy a healthy, active life. Our goal is to provide comprehensive, child-friendly care tailored to each patient’s needs.