চোখের প্যাথলজি ছাড়া দৃষ্টিশক্তি আংশিক বা মোট ক্ষতি; অক্ষিস্নায়ু বা অক্ষিপট বা মস্তিষ্কের রোগ দ্বারা সৃষ্ট

amaurosis's Usage Examples:

Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life.

Amaurosis fugax (Greek amaurosis meaning darkening, dark, or obscure, Latin fugax meaning fleeting) is a painless temporary loss of vision in one or both.

Lebercilin, also known as leber congenital amaurosis 5 (LCA5), is a protein that in humans is encoded by the LCA5 gene.

Leber congenital amaurosis primarily affects the retina, and typically severe visual impairment begins.

gene are associated with photoreceptor degeneration, Leber's congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2.

person would visit a doctor and complain as follows: "Doctor, I have amaurosis fugax.

Defects in the gene result in the Leber congenital amaurosis (LCA) syndrome and in the eye disease glaucoma.

however human clinical trials for both choroideremia and Leber's congenital amaurosis (LCA) have produced somewhat promising results.

membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary.

severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis.

Luxturna, is a gene therapy medication for the treatment of Leber congenital amaurosis.

amaurosis's Meaning':

partial or total loss of sight without pathology of the eye; caused by disease of optic nerve or retina or brain