“…They are a heterogenous group of disorders with multiple underlying mechanisms and may be sporadic or inherited. Notable conditions include coloboma (incomplete closure of the embryonic cleft), staphyloma (excavation of the peripapillary area), optic nerve choristoma (a congenital ocular or periocular tumour), tumours of the optic nerve and sheath (glioma, meningioma, medulloepithelioma, oligodendroglioma), morning glory syndrome (an embryological malformation of the optic disc) and myelinated nerve fibres (optic nerve fibres at the level of the optic disc are typically unmyelinated) (239,240). The following sections focus on OND relevant to my study population and systematic literature review, and as such describe optic nerve hypoplasia (ONH), septo-optic dysplasia (SOD), primary congenital glaucoma and buphthalmos, and optic neuropathy associated with retinopathy of prematurity (ROP).…”