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Updated: Apr 27, 2026

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Tuberous sclerosis presenting with acute kidney failure, pyelonephritis, and polycystic kidney disease
Masoumeh Mohkam1, Shirin Shohadaii, Farshid Kompani
1Pediatric Nephrology Research Center; Division of Pediatric Nephrology, Shahid Beheshti University of Medical Sciences; Tehran, Iran. mohkam@pirc.ir.
Abstract:
Tuberous sclerosis complex (TSC) is a multisystemic inherited autosomal dominant disease characterized by the development of hamartomas in the brain and kidneys. In about 2% of patients, polycystic kidney disease is present, which may result in different stages of renal insufficiency. Acute kidney failure has not been reported in infants with TSC. We report a female infant with TSC who was admitted to hospital with pyelonephritis, acute kidney injury, and polycystic kidney disease.
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