Multicystic renal dysplasia, bilateral

Common Name(s)

Multicystic renal dysplasia, bilateral

Congenital anomalies of the kidneys and urinary tract (CAKUT) encompasses a spectrum of developmental disorders of the urinary tract that can range from mild vesicoureteral reflux to severe renal agenesis. Other phenotypes include renal duplication, small kidneys, ureteropelvic junction obstruction, hydronephrosis, and renal dysplasia. These abnormalities can result in kidney damage, and possibly renal failure (summary by {19:Vivante et al., 2015}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Multicystic renal dysplasia, bilateral" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
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The terms "Multicystic renal dysplasia, bilateral" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.