Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

BACKGROUND: Li–Fraumeni syndrome (LFS) is a rare autosomal hereditary predisposition to multiples cancers, mainly affecting young individuals. It is characterized by a broad tumor spectrum. To our best knowledge, only one Tunisian study with a confirmed LFS was published. METHODS: Our study focused...

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Detalles Bibliográficos
Autores principales: Sassi, Hela, Meddeb, Rym, Cherif, Mohamed Aziz, Nasr, Chiraz, Riahi, Aouatef, Hannachi, Samia, Belguith, Neila, M’rad, Ridha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895785/
https://www.ncbi.nlm.nih.gov/pubmed/35246108
http://dx.doi.org/10.1186/s12920-022-01189-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895785/
https://www.ncbi.nlm.nih.gov/pubmed/35246108
http://dx.doi.org/10.1186/s12920-022-01189-w

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