Medulloblastoma in a toddler with Gorlin syndrome

Gorlin syndrome (GS) is a rare hereditary multisystem disorder caused by mutations in PTCH1, PTCH2, or SUFU. It is characterized by multiple anomalies and an increased risk of developing various tumors. Basal cell carcinoma is most common, and medulloblastoma (MB) is especially frequent in patients...

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Detalles Bibliográficos
Publicado en:Proc (Bayl Univ Med Cent)
Autores principales: Al-Rahawan, Mohamad G., Trevino, Sorleen, Jacob, Roy, Murray, Jeffrey C., Al-Rahawan, Mohamad M.
Formato: Artigo
Lenguaje:Inglês
Publicado: Taylor & Francis 2018
Materias:
Case Studies
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5914436/
https://ncbi.nlm.nih.gov/pubmed/29706825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/08998280.2018.1435111
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