Novel PHOX2B germline mutation in childhood medulloblastoma: a case report

ConclusionsThis case revealed a de novoPHOX2B germline mutation as a potential cause of medulloblastoma in a child and suggests familial germline variant screening is useful when an affected family is considering having a second child.

Source: Hereditary Cancer in Clinical Practice - January 19, 2021 Category: Cancer & Oncology Source Type: research