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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,...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Case Rep Pediatr |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Hindawi
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7814941/ https://ncbi.nlm.nih.gov/pubmed/33505750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6612802 |
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