Pediatric Case of Li–Fraumeni Syndrome in Honduras

Li–Fraumeni syndrome is an inherited, autosomal dominant disease. It is categorized as a rare disease caused by mutations of the TP53 gene, which causes increased susceptibility of the patients and their children to many types of cancer. Choroid plexus tumor is rare, which occurs in 0.3 cases per 1,...

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Detalles Bibliográficos
Autores principales: Martínez-Beckerat, R., Alas-Pineda, C., Melgar-Gonzales, M., Mejía-Raudales, B., Andino-Paz, N., Bejarano-Cáceres, S., Chiang, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814941/
https://www.ncbi.nlm.nih.gov/pubmed/33505750
http://dx.doi.org/10.1155/2021/6612802

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814941/
https://www.ncbi.nlm.nih.gov/pubmed/33505750
http://dx.doi.org/10.1155/2021/6612802

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