Mechanism of renal cyst formation in a child with tuberous sclerosis complex: a case report

Abstract Background Tuberous sclerosis complex (TSC) is a multisystem genetic disorder characterized by the development of benign tumors in various organs, including the brain, kidneys, heart, lungs, skin, and eyes. Herein, an infant who was followed up with a diagnosis of TSC and multiple cysts whi...

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Autori principali:	Ece Koç, Emre Leventoğlu, Akif Kavgacı, Alev Elçi Karaduman, Tuğba Hirfanoğlu, Kibriya Fidan
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	SpringerOpen 2024-09-01
Serie:	Egyptian Pediatric Association Gazette
Soggetti:	Tuberous sclerosis complex Autosomal dominant polycystic kidney disease Contiguous gene syndrome
Accesso online:	https://doi.org/10.1186/s43054-024-00310-1
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