article · Clinical Case Reports
The coexistence of tuberous sclerosis complex (TSC) with a congenital solitary kidney is exceptionally rare and worsens prognosis. This combination increases the risk of renal failure, requiring meticulous monitoring, tailored surveillance, and renal preservation strategies. Early recognition, multidisciplinary care, and individualized management are essential to optimize outcomes in complex clinical scenarios.
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DOI: 10.1002/ccr3.73255
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