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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Detalles Bibliográficos
Autores principales: Lonati, Chiara, Simeone, Claudio, Suardi, Nazareno, Spiess, Philippe E., Necchi, Andrea, Moschini, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Second Military Medical University 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643301/
https://www.ncbi.nlm.nih.gov/pubmed/36381590
http://dx.doi.org/10.1016/j.ajur.2022.05.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643301/
https://www.ncbi.nlm.nih.gov/pubmed/36381590
http://dx.doi.org/10.1016/j.ajur.2022.05.009

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