IMPE Abstracts

Septo‐optic dysplasia (SOD) or Morsier's syndrome is a congenital developmental anomaly of the brain that could present absent of septum pellucidum and corpus callosum, optic nerve hypoplasia and pituitary hypoplasia. Gene variants of the transcription factors HESX1 SOX3, SOX2, and OTX2 had been described in SOD. The two latter are also causatives genes of anophthalmia. Craniopharyngioma (CP) is a tumor with low histological grade, the association to unilateral anoph...