An X-linked recessive retinal disease characterized by fundus hypopigmentation, decrased visual acuity, nystagmus, astigmatism, progressive axial myopia, defective dark adaptation and protanopia.
A type of astigmatism associated with abnormal curvatures on the anterior and/or posterior surface of the cornea.
|
Total: 0
|
|
|
(per page)
|
