Congenital single kidney in tuberous sclerosis complex (Bourneville disease)

CONCLUSION: This case report highlights Bournevile disease in a patient with a congenital single kidney, a rare finding that further complicates the disease. It emphasises the importance of recognising and managing this condition to ensure appropriate care for affected individuals.PMID:38576950 | PMC:PMC10990388 | DOI:10.1097/MS9.0000000000001834
Source: Annals of Medicine - Category: Internal Medicine Authors: Source Type: research