medullary cystic disease
Quick Summary
Medullary cystic disease is a congenital condition where cysts form in the kidney's small collecting tubules. These tubules transport urine from the nephrons, the kidney's urine-producing units. The disease typically lacks warning signs, but affected individuals may develop anemia, low blood salt concentrations, and elevated nitrogenous substances in their blood. The kidneys often shrink, develop a granular surface, and show numerous small cysts alongside significant scar tissue. This condition most commonly affects older children and young adults.1
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