Progress in Tuberous Sclerosis Complex Renal Disease
Author:
Abstract
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder that affects both fetal development and postnatal tissue growth, resulting in altered brain structures and a tumor predisposition syndrome. Although every organ system is affected by the disease, kidney involvement is a leading cause of death in adults with TSC. Over the past decade, significant progress has been made in understanding the renal disease. This review focuses on the cystic and solid renal lesions in TSC, including their pathobiology and treatment.
Publisher
Begell House
Subject
Cancer Research
Link
https://www.dl.begellhouse.com/download/article/2aefc98246e73fd6/CRO-42857.pdf
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1. The extent of kidney involvement in paediatric tuberous sclerosis complex;Pediatric Nephrology;2024-06-04
2. Carbonic Anhydrase 2 Deletion Delays the Growth of Kidney Cysts Whereas Foxi1 Deletion Completely Abrogates Cystogenesis in TSC;International Journal of Molecular Sciences;2024-04-27
3. Clinical practice recommendations for kidney involvement in tuberous sclerosis complex: a consensus statement by the ERKNet Working Group for Autosomal Dominant Structural Kidney Disorders and the ERA Genes & Kidney Working Group;Nature Reviews Nephrology;2024-03-05
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