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 · pp. 33–37 · Published 1 May 2025
10.9734/ijmpcr/2025/v18i2419Abstract
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.
Cited by 0
No indexed citations yet.
Related research
- Tachyphylaxis to ranibizumab in the Treatment of Age-related Macular Degeneration — shares topic coverage
- Bilateral Asymmetric Best Vitelliform Macular Dystrophy in Adulthood: Insights from Multimodal Imaging — shares topic coverage
Article metrics
Real usage data collected on this platform.
0
Page views
0
PDF downloads
0
Outbound clicks
0
Citations
Views by country
Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".
No views recorded yet.
Traffic sources
Referring site, by host.
No traffic recorded yet.
Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.