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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Proc (Bayl Univ Med Cent)
Egile Nagusiak: Al-Rahawan, Mohamad G., Trevino, Sorleen, Jacob, Roy, Murray, Jeffrey C., Al-Rahawan, Mohamad M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Taylor & Francis 2018
Gaiak:
Case Studies
Sarrera elektronikoa: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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