Case Report of Malattia Leventinese Complicated by Choroidal Neovascularization: A Genetic Perspective
Elkhoyaali A *
Military Training Hospital Mohammed V Rabat, Morocco.
Laaouina S
Military Training Hospital Mohammed V Rabat, Morocco.
Chaibi Z
Military Training Hospital Mohammed V Rabat, Morocco.
Achegri Y
Military Training Hospital Mohammed V Rabat, Morocco.
Fiqhi A
Military Training Hospital Mohammed V Rabat, Morocco.
Mouzari.Y
Military Training Hospital Mohammed V Rabat, Morocco.
*Author to whom correspondence should be addressed.
Abstract
Malattia Leventinese (ML) is an autosomal dominant macular dystrophy with a homogeneous genetic makeup. From an ophthalmic perspective, it can be identified by a radial arrangement of parapapilla deposits, also known as Forni's verrucosities, and by drusen-like deposits in the macula.
Keywords: Malattia levenetinese, dominant familial drusen, choroidal neovascularization, macular oct, anti vegf injections