A Case of Bilateral Pseudo Papilledema Revealing a Leber’s Hereditary Optic Neuropathy

Leber Hereditary Optic Neuropathy (LHON) is a mitochondrial disease caused by mutations in DNA affecting the respiratory complex I and leading to death of retinal ganglion cells (RGCs) [1]. It characterized sudden onset usually severe bilateral loss central vision, predominantly young men [2]. The risk vision 50% among 10% women who carry LHON primary [3]. We report an atypic case 11 years old girl.