Genitourinary manifestations of Lynch syndrome in the urological practice

Objective: Lynch syndrome (LS) is an autosomal dominant hereditary disorder resulting from germline mutation in at least one of the four mismatch repair genes or in EPCAM gene. From a clinical perspective, LS patients exhibit an increased predisposition to multiple primary malignancies and early age...

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Autors principals:	Chiara Lonati, Claudio Simeone, Nazareno Suardi, Philippe E. Spiess, Andrea Necchi, Marco Moschini
Format:	Artigo
Idioma:	Inglês
Publicat:	Elsevier 2022-10-01
Col·lecció:	Asian Journal of Urology
Matèries:	Hereditary disease Hereditary nonpolyposis colorectal cancer Lynch syndrome Mismatch repair Upper tract urothelial carcinoma
Accés en línia:	http://www.sciencedirect.com/science/article/pii/S2214388222000959
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