PTCH1 mutant small cell glioblastoma in a patient with Gorlin syndrome: A case report
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DOI: 10.3892/ol.2022.13446
Abstract: Gorlin syndrome or nevoid basal cell carcinoma syndrome is a rare genetic disease characterized by predisposition to congenital defects, basal cell carcinomas and medulloblastoma. The syndrome results from a heritable mutation in PATCHED1 (PTCH1), causing… read more here.
Keywords: cell; cell glioblastoma; patient gorlin; small cell ... See more keywords