Neurofibromatosis type 1: Sophie’s story
Neurofibromatosis type 1: Sophie’s story (French only)
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Neurofibromatosis type 1 (NF1) is a genetic disorder that primarily affects the skin and nervous system. Depending on the case, several other systems may also be affected. In Sophie’s case, the CHU Sainte-Justine team is keeping a close eye on her eyesight. A tumour called an optic nerve glioma is threatening her vision. The multidisciplinary neurofibromatosis clinic at CHU Sainte-Justine invites you to discover her story and this facet of the disease.