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Fiqhi A

Publications (1)

Case Report of Malattia Leventinese Complicated by Choroidal Neovascularization: A Genetic Perspective

Elkhoyaali A, Laaouina S, Chaibi Z, Achegri Y, Fiqhi A & Mouzari.Y · International Journal of Medical and Pharmaceutical Case Reports · 2025

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 ma...

Open access Research Article 10.9734/ijmpcr/2025/v18i2419