Two Novel CAPN5 Variants Associated with Mild and Severe Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Phenotypes.

: We report two new CAPN5 mutations associated with a phenotype of Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy. : We performed next generation sequencing in two patients with ADNIV phenotype; the variants identified were explored further. : Patient 1 was heterozygous for CAPN5 c.