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WNT Medulloblastoma

Very good prognosis

Long-term survival > 90%

Majority have classical histology

Beta-catenin nucleo-positivity,

CTNNB1

gene

mutations, and monosomy 6

Rarely the WNT subgroup may include large

cell/anaplastic cases. Can occur at all ages, but is

infrequent in infants

M:F ratio approximately 1:1