Graves’ disease in children is considered rare, these children can present ocular attacks related to this pathology .We report the case of a girl presenting an exophthalmia complicated by corneal attack in the framework of a graves' disease. Our 6-year-old patient was admitted t...
Birdshot chorioretinopathy is a well-known yet poorly studied form of posterior uveitis characterized by multiple, distinct, hypopigmented choroidal lesions and strongly associated with human leukocyte antigen (HLA)-A29. We report the case of a 54-year-old woman with no particula...
Dominant optic atrophy (DOA) orKjer's disease, caused by mutations in the OPA1 gene, is an autosomal dominant inherited pathology due to degeneration of retinal ganglion cells leading to loss of optic nerve axons. It manifests itself in atrophy of the optic nerve head, which, tog...
Best macular dystrophy, also called vitelliform macular dystrophy, is an autosomal dominant disease described by Frederick Best in 1905. It classically occurs in childhood and is characterized by macular deposits of vitelline material. We report the case of a 5-year-old female pa...
Secondary glaucoma is a serious complication in patients who have already undergone surgery for congenital cataract. We report the case of a 27 year old female patient, operated on at the age of 3 weeks for bilateral congenital cataract, subsequently complicated by secondary glau...