Genetic Polymorphisms in VEGFR Coding Genes (<i>FLT1</i>/<i>KDR</i>) on Ranibizumab Response in High Myopia and Choroidal Neovascularization Patients

• Päätekijät: David Blánquez-Martínez (Tekijä), Xando Díaz-Villamarín (Tekijä), Sonia García-Rodríguez (Tekijä), Alba Antúnez-Rodríguez (Tekijä), Ana Pozo-Agundo (Tekijä), Luis Javier Martínez-González (Tekijä), José Ignacio Muñoz-Ávila (Tekijä), Cristina Lucía Dávila-Fajardo (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: MDPI AG, 2022-07-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

A severe form of myopia defined as pathologic/high myopia is the main cause of visual impairment and one of the most frequent causes of blindness worldwide. It is characterized by at least 6 diopters or axial length (AL) of eyeball > 26 mm and choroidal neovascularization (CNV) in 5 to 10% of cas...