WebOptic nerve hypoplasia can also be associated with unusual side-to-side eye movements (nystagmus) and other eye abnormalities. The second characteristic feature of septo-optic dysplasia is the abnormal development of structures separating the right and left halves of the brain. These structures include the corpus callosum, which is a band of ... WebOptic nerve (ON) aplasia is a rare congenital anomaly. It is characterised by the absence of optic nerve, nerve fibre layer, ganglion cells, and retinal blood vessels. ON aplasia is usually unilateral. Bilateral cases are very rare. We report such a rare case with bilateral ON aplasia and corpus callosum hypogenesis.
Aplasia: Definition, Types & Causes - Cleveland Clinic
WebAug 13, 2024 · Aplasia — Optic nerve aplasia is an extremely rare, nonhereditary occurrence of unknown etiology. It is characterized by complete lack of the optic nerve, disc, retinal nerve fiber layer, ganglion cells, and retinal vasculature [ 1,2 ]. Optic nerve aplasia typically is associated with a variety of other ocular malformations, including ... WebFeb 22, 2024 · Morning glory syndrome (MGS) is a congenital optic disc pathology.[1] It was first described in 1970 by Kindler.[2] He reported ten cases of congenital optic disc anomaly. The optic nerve head was funnel-shaped. It had a central whitish fibrous tissue and was surrounded by a ring-shaped area of chorioretinal pigmentary disturbance. The retinal … slughorn book
Case report: Unilateral optic nerve aplasia and developmental …
WebJul 1, 2014 · Optic nerve (ON) aplasia is a rare developmental anomaly comprising of absence of the ON, ganglion cells and the central retinal vessels. It is usually accompanied by a variety of central nervous system (CNS) malformations. We report an extremely rare case of bilateral true ON aplasia occurring as an isolated CNS anomaly. WebMay 14, 2024 · Aplasia of the optic nerve and eye are rare ( Fig. 46.6 ). This occurs sporadically due to failure to form the optic vesicle. Absence of eye development results in concomitant orbital hypoplasia and facial deformity. 4 Leber hereditary optic neuropathy (LHON) eventually leads to bilateral optic nerve atrophy ( Fig. 53.6 ). slughorn crossword clue