Renal agenesis, bilateral is a rare congenital condition characterized by the absence of both kidneys in a newborn. It occurs when the kidneys fail to develop during fetal growth, leading to a complete absence of renal tissue. This condition affects approximately 1 in 3,000 to 5,000 live births.
Bilateral renal agenesis often results in severe complications and is incompatible with life. However, in some cases, it may be associated with other congenital abnormalities that can impact the overall prognosis.
Although bilateral renal agenesis is a devastating condition, advancements in medical technology and prenatal care have enabled early detection and improved management strategies. Genetic counseling is highly recommended for families affected by renal agenesis, bilateral to provide support and information.
In conclusion, bilateral renal agenesis is a rare congenital condition characterized by the absence of both kidneys. It is important to raise awareness about this condition and emphasize the need for early diagnosis and appropriate medical care to improve outcomes for affected infants.
Renal agenesis, bilateral is a rare congenital condition where both kidneys fail to develop properly during fetal growth. This condition can have significant impacts on the affected individuals, requiring immediate medical attention and ongoing treatment. Here are some treatment options available for individuals diagnosed with bilatera...
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