Case Report of Malattia Leventinese Complicated by Choroidal Neovascularization: A Genetic Perspective
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.
Authors
- Aissam Fiqhi
- A. Elkhoyaali (ORCID: https://orcid.org/0000-0002-1307-3597)
- Zakaria Chaibi
- Soukaina Laaouina - (ORCID: https://orcid.org/0009-0008-5928-477X)
- M Y
- Youssef Achegri (ORCID: https://orcid.org/0009-0007-6991-1776)
Publication Details
- Journal
- International Journal of Medical and Pharmaceutical Case Reports
- Published
- 2025-05-01
- DOI
- https://doi.org/10.9734/ijmpcr/2025/v18i2419
- Primary Topic
- melanin and skin pigmentation
- Type
- article
- Field-Weighted Citation Impact
- 0.00