Index Leber hereditary optic neuropathy (from the English Leber Hereditary Optic Neuropathy –…
Index Leber's congenital amaurosis is the name given to a group…
Autosomal dominant optic atrophy (ADOA) is a rare genetic mitochondrial disease, (with…
Contents Cone dystrophies comprise a heterogeneous group of disorders characterized by…
Contents Choroideremia (CHM) is a progressive, bilateral form of chorioretinal dystrophy, characterized…
X-linked retinoschisis, or X-linked juvenile retinoschisis (congenital X-linked retinoschisis…
Contents Dominant familial drusen share some characteristics of age-related macular degeneration.…
Stargardt disease is the most common form of macular dystrophy…
Retinitis Pigmentosa (RP) is a clinically and genetically heterogeneous group of…