The findings support a potential role for MC1R as a candidate modifier interacting with TYR in neuroretinal development and incorporate MC1R screening in patients with unresolved foveal hypoplasia to help clarify complex oligogenic mechanisms and optimize phenotypic classification.
E. Di Iorio, Francesco Parmeggiani, Antonella De Nardi et al.· Genes· 0 citations
A multidisciplinary group of experts from eight European countries developed a clinical consensus statement (CCS), using a modified Delphi process, that provides guidance on evaluation of primary visual functions in children with low vision, regardless of etiologies.
A. Suppiej, C. Ceccato, R. Maggi et al.· Survey of ophthalmology· 0 citations
PVR and high myopia are confirmed as risk factors for recurrent RRD and suggests preoperative glaucoma and systemic hypertension as additional predictors of recurrence and the importance of risk stratification in guiding individualized surgical planning, intensified early postoperative surveillance, and long-term follo...
Chiara Vivarelli, Marco Pellegrini, P. M. Talli et al.· BMC Ophthalmology· 0 citations
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