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</html><thumbnail_url>https://retinaclub.es/wp-content/uploads/2025/09/A-3.jpeg</thumbnail_url><thumbnail_width>983</thumbnail_width><thumbnail_height>991</thumbnail_height><description>Albinism is a genetic disorder characterized by hypopigmentation, both cutaneous and ocular, due to impaired melanin biosynthesis. There are oculocutaneous and isolated ocular forms (less frequent). The seven variants of oculocutaneous albinism are inherited in an autosomal recessive pattern and affect both sexes equally. The two variants with exclusive ocular involvement are inherited in an [&hellip;]</description></oembed>
