Oct 2026
Bi-Allelic PRKCZ Loss-of-Function Variants and Adult-Onset Retinitis Pigmentosa.
Viviana Cordeddu, Riccardo Sangermano, Sterre W. M. Mulder et al.
· JAMA ophthalmology · 0 citations
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Open access
Aug 2026
Monotherapy or combination therapy for myopia control: a structured narrative comparison of 12-month axial elongation
ABSTRACT Purpose: To compare annual axial elongation in children treated with low-dose atropine (0.01%) combined with optical interventions versus higher-dose atropine (≥0.05%) monotherapy and to assess whether combination therapy provides a clinically meaningful advantage over single-agent pharmacologic treatment. Met...
J. Polling, D. V. van Hemert, Hozan Zebari et al.
· Strabismus · 0 citations
Open access
Aug 2026
The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations
Findings further support AP5B1 as a cause of macular dystrophy, identify p.(Leu785Pro) as a relatively frequent pathogenic allele in individuals of European and Ashkenazi Jewish ancestry, and expand the associated phenotypic spectrum to include both isolated macular dystrophy and possible syndromic presentations.
Petra Liskova, L. Dudakova, Karolina Kaminska et al.
· HGG advances · 0 citations