Browsing by Author "897042f6-2066-4542-8ed4-39c37db11c12"
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Nakousi Capurro, Nicole; Huserman, Jonathan; Castillo, Silvia; Gavia Herrera, Luisa; Romero, Pablo; Pizarro, Felipe; Quezada, Cristian; Cea, Francisco (Wiley, 2020)Knobloch Syndrome (KS) is a rare autosomal recessive hereditary disease. Despite its clinical heterogeneity, it is characterized by vitreoretinal degeneration and high myopia, with or without occipital skull defects. It ...