Between 1 in 1,000 and 1 in 4,300 babies are born with MCDK each year.
01 | Introduction
Multicystic dysplastic kidney (MCDK) is a pediatric renal condition in which one or both kidneys do not develop normally in the womb. Instead of ordinary kidney tissue, multiple cysts develop, causing the kidney to be nonfunctional. In a majority of cases, only one kidney is affected, and the other, healthy kidney will grow larger to compensate for the cystic one. The nonfunctioning kidney may shrink and disappear by the time the child is five years old.
02 | Symptoms
MCDK usually does not cause any symptoms, but because one kidney does not work, children born with this condition may have a higher risk of urinary tract infections and high blood pressure when they become adults. Other urinary tract problems affecting the working kidney can increase the risk of developing chronic kidney disease.
03 | Types
Two types of MCDK can occur:
04 | Diagnosis
Most cases of MCDK are diagnosed before birth, during a prenatal ultrasound at around 20 weeks into the pregnancy. In an ultrasound, the kidney will appear as several cysts with no surrounding functioning kidney. MCDK can also be detected by measuring the levels of amniotic fluid. After birth, further ultrasounds, MRI, or CT scans may be used to confirm the diagnosis.
Learn More
For more information on MCDK and supportive resources, please visit niddk.nih.gov.
References
https://www.childrenshospital.org/conditions/multicystic-dysplastic-kidney
https://www.chop.edu/conditions-diseases/multicystic-dysplastic-kidney
https://infokid.org.uk/conditions/multicystic-dysplastic-kidney-mcdk/
https://pmc.ncbi.nlm.nih.gov/articles/PMC10195076/
https://www.medicalnewstoday.com/articles/multicystic-dysplastic-kidney