A rare progressive eye disorder caused by a genetic defect on chromosome 11p13-p12. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. See also Exudative vitreoretinopathy 3
As scientists who evolve with technology we treat innovation as a way of life, a life we dedicate to improvement and advancement of Safety, Health and Environment.
