amaurosis मीनिंग इन हिंदी

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अधिक: आगे

Those experiencing amaurosis usually experience complete symptom resolution within a few minutes.
Leber's congenital amaurosis appears to be inherited in this fashion.
From this he was blinded by the illness called amaurosis.
When investigating amaurosis fugax, an ophthalmologic consult is absolutely warranted if available.
Leber congenital amaurosis ( LCA ) is an inherited disorder that causes vision loss.
Most episodes of amaurosis fugax are the result of stenosis of the ipsilateral carotid artery.
In a small minority of those who experience amaurosis, stroke or permanent vision loss results.
Leber's congenital amaurosis is an inherited blinding disease caused by mutations in the RPE65 gene.
Mutations in this gene result in Leber's congenital amaurosis and cone-rod dystrophy-6 diseases.
A mutation in this gene leads to infant and child blindness, a disease known as Leber Congenital Amaurosis.

संज्ञा.

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