Congenital medulloblastoma in two brothers with SUFU-mutated Gorlin-Goltz syndrome: Case reports and literature review

BACKGROUND: Congenital medulloblastoma is very rare, and many cases involve germline mutations that can lead to inherited syndromes. Here, we first report two brothers with congenital medulloblastoma who were diagnosed with Gorlin-Goltz syndrome caused by SUFU mutation. CLINICAL PRESENTATION: Medull...

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Detalles Bibliográficos
Autores principales: Chen, Yufan, Zhang, Haibo, Zhao, Yang, Ma, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9603755/
https://www.ncbi.nlm.nih.gov/pubmed/36313636
http://dx.doi.org/10.3389/fonc.2022.988798

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9603755/
https://www.ncbi.nlm.nih.gov/pubmed/36313636
http://dx.doi.org/10.3389/fonc.2022.988798

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