[Ocular alterations in patients with Alport syndrome-An update].
Kristina HessOliver GrossSebastian BemmePeter MeyerPatricia TakeJan BoeckhausFrank G HolzNicolas FeltgenPublished in: Die Ophthalmologie (2023)
The AS can manifest in various structures of the eye. The staircase-like changes of the central retina in AS patients indicate the important role of collagen type IV in the homeostasis and regular function of the inner retinal layers. The often mild foveal hypoplasia may provide clues to the role of collagen type IV in retinal embryogenesis. While anterior lenticonus is pathognomonic for AS and can be treated easily by refractive lens exchange, the only option currently available for retinal alterations is close follow-up and, if necessary, treatment of systemic complications of AS.