Related Experiment Video
Updated: Mar 3, 2026

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Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
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Multicystic Kidney Disease in a Family With Tuberous Sclerosis Complex
Julia S Donald1, Caitlin Edmonstone2, Denise L Chan2,3
1Nephrology, Sydney Children's Hospital, Randwick, Australia.
Nephrology (Carlton, Vic.)
|March 1, 2026
Summary
Tuberous Sclerosis Complex (TSC) can cause kidney disease, even with TSC1 variants, not just TSC2. This family study highlights the risk of progressive kidney disease and the need for renal monitoring in all TSC patients.
Area of Science:
- Genetics
- Nephrology
- Medical Genetics
Background:
- Tuberous Sclerosis Complex (TSC) is a genetic disorder affecting multiple organs, often involving the TSC1 or TSC2 genes.
- Kidney issues in TSC commonly include angiomyolipomas (AMLs) and cysts, particularly with TSC2 variants.
- Severe polycystic kidney disease and end-stage kidney disease (ESKD) are typically associated with TSC2/PKD1 contiguous gene deletions.
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